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Blackpill autism is a symptom of bad genetics

  • Thread starter DisposableMale01
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DisposableMale01

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http://crackingtheenigma.blogspot.com/2011/10/many-faces-of-autism.html

"The press release from the University of Missouri summarises the results as follows:
  • Children with autism have a broader upper face, including wider eyes.
  • Children with autism have a shorter middle region of the face, including the cheeks and nose.
  • Children with autism have a broader or wider mouth and philtrum -- the divot below the nose, above the top lip."
I literally don't know any attractive autists. seems autism doesn't only make your socially inept, but ugly, too. it's OVER for autistic-cels.
 
I literally don't know any attractive autists. seems autism doesn't only make your socially inept, but ugly, too. it's OVER for autistic-cels.
I knew an attractive Autistic Negro Girl. She looked like Donna Summer. I wanted her so bad. Her voice was like Marylin Monroe. You have to see her to believe her. She wasn't really interested in me. I was crushed when she chose a (disabled) Black Man over me. I would get erections just thinking about her. If that didn't make me rope, nothing will.
 
I didn’t know this, thanks for sharing I guess...:feelsbadman:

I thought it only made me act retarded but it’s also the reason I’m ugly. Damn.
 
http://crackingtheenigma.blogspot.com/2011/10/many-faces-of-autism.html

"The press release from the University of Missouri summarises the results as follows:
  • Children with autism have a broader upper face, including wider eyes.
  • Children with autism have a shorter middle region of the face, including the cheeks and nose.
  • Children with autism have a broader or wider mouth and philtrum -- the divot below the nose, above the top lip."
I literally don't know any attractive autists. seems autism doesn't only make your socially inept, but ugly, too. it's OVER for autistic-cels.
:feelsbadman::feelscry::feelsrope:
 
I didn’t know this, thanks for sharing I guess...:feelsbadman:

I thought it only made me act retarded but it’s also the reason I’m ugly. Damn.
God scammed you bruh.
 
Well I'm still ugly without autism
 
Probiotics can cure autism
 
lookism is full of gl autists
 
Not surprising.
The older the woman the higher the chance of the good old tism
 
I know an autist who is like 6'4. That alone makes him chadlite.
 
This ruins everything. Personality is back to being 100 percent cope. The reason why most autistic people can't get laid is because being autistic makes you ugly and not because it affects your personality.
 
Bears shit in the woods.
 
I have autism and I’ve been called handsome many times online and in person by decent looking girls. I can never force them to give me what I want because it’s impossible for me to control a social situation.
 
Yes, of-course. I am enrolled in a study for patients with ASD. Please observe this long post.

SPARK:


SPARK, the world’s largest autism research study, is part of the Simons Foundation Autism Research Initiative, or “SFARI.”

Marilyn and Jim Simons founded the Simons Foundation over 26 years ago to advance basic science — science that uncovers how the world works. The Simons family provides all funding for the foundation, so the foundation — and SPARK —do not need to fundraise. The foundation has $4.6 billion in assets for its work.

About 15 years ago, the Simons saw that not much was understood scientifically about autism, even though so many people are affected by it. Because they had a family member with autism, they decided to help fund research in this area. In 2006, the Simons Foundation launched SFARI to improve the understanding, diagnosis, and treatment of autism spectrum disorders. Today, SFARI is one of the world’s largest autism research funders, supporting scientists around the globe trying to understand the disorder.

When SFARI began, its team knew that one powerful way to investigate autism is through genetics. However, genetic studies require large numbers of participants and recruitment is a huge and expensive task for researchers. So SFARI’s first major project was to recruit 2,500 families with a child on the autism spectrum. Together, these families and their genetic information, or data, are called the Simons Simplex Collection, or SSC. The SSC is now a permanent repository of genetic samples and data that are available for free to all qualified researchers. This was SFARI’s first collection of family genomes, and it proved to be invaluable to a new generation of autism researchers, launching much new work.

In 2011, SFARI launched the Simons Variation in Individuals Project to better understand genetic neurodevelopmental conditions, specifically those associated with autism. This project became affiliated with SPARK and was renamed Simons Searchlight. Simons Searchlight brings together families that have the same genetic diagnosis, so that they may share experiences, learn and create a community.

Spark


Gene List:

Date Revised: October 4, 2021


What genes and genetic differences are linked to autism?​


The SPARK gene list includes genes and specific genetic differences scientists can confidently say are related to autism. New genes and gene changes are added to this list twice a year. The list is vetted by SPARK researchers and a committee of genetics experts. View a SPARK video about this process.


What is a “genetic difference”? What type of genetic differences will SPARK uncover?​


Our genes contain the instructions, or code, that tell our cells how to grow, develop and work. “Genetic difference” refers to a change in a gene. These differences can range from being harmful to helpful. Some can have no effect.


Once our lab receives a family’s samples, we look for genetic differences that are definitively linked to autism. If such changes are found and confirmed, the family is contacted about those results. SPARK will return the genetic result either through a SPARK genetic counselor or through the family’s own medical provider.


Since new autism genes are discovered every year, each family’s genes will be re-analyzed every year and rechecked for results.



The gene of note, for myself, appears to be TCF4. I haven't yet received SPARK results, yet I have results from both genotyping assays and Whole Genome Sequencing(Nebula/Akesogen).

Rs9960767

(AncestryDNA/LivingDNA/23&Me/Vitagene)

CC TCF4

(Nebula)

TC

(https://gene.sfari.org/database/human-gene/TCF4)


The population frequency is quite low:

PopulationGroupSample SizeRef AlleleAlt Allele

PopulationGroupSample SizeRef AlleleAlt Allele
Total Global97800A=0.93291C=0.06709, G=0.00000
European Sub80228A=0.94664C=0.05336, G=0.00000
African Sub6000A=0.8507C=0.1493, G=0.0000
African Others Sub202A=0.827C=0.173, G=0.000
African American Sub5798A=0.8515C=0.1485, G=0.0000
Asian Sub224A=1.000C=0.000, G=0.000
East Asian Sub184A=1.000C=0.000, G=0.000
Other Asian Sub40A=1.00C=0.00, G=0.00
Latin American 1 Sub222A=0.968C=0.032, G=0.000
Latin American 2 Sub1176A=0.9558C=0.0442, G=0.0000
South Asian Sub4918A=0.8015C=0.1985, G=0.0000

There is also the uncommon MET variant:
Met Med


GG


PopulationGroupSample SizeRef AlleleAlt Allele

PopulationGroupSample SizeRef AlleleAlt Allele
Total Global18518C=0.57436G=0.42564
European Sub14150C=0.54580G=0.45420
African Sub2898C=0.7502G=0.2498
African Others Sub114C=0.798G=0.202
African American Sub2784C=0.7482G=0.2518
Asian Sub112C=0.384G=0.616
East Asian Sub86C=0.36G=0.64


 
Yes, of-course. I am enrolled in a study for patients with ASD. Please observe this long post.

SPARK:




View attachment 598601

Gene List:





The gene of note, for myself, appears to be TCF4. I haven't yet received SPARK results, yet I have results from both genotyping assays and Whole Genome Sequencing(Nebula/Akesogen).

View attachment 598603
(AncestryDNA/LivingDNA/23&Me/Vitagene)

View attachment 598606
(Nebula)

View attachment 598614
(https://gene.sfari.org/database/human-gene/TCF4)


The population frequency is quite low:

PopulationGroupSample SizeRef AlleleAlt Allele

PopulationGroupSample SizeRef AlleleAlt Allele
Total Global97800A=0.93291C=0.06709, G=0.00000
European Sub80228A=0.94664C=0.05336, G=0.00000
African Sub6000A=0.8507C=0.1493, G=0.0000
African Others Sub202A=0.827C=0.173, G=0.000
African American Sub5798A=0.8515C=0.1485, G=0.0000
Asian Sub224A=1.000C=0.000, G=0.000
East Asian Sub184A=1.000C=0.000, G=0.000
Other Asian Sub40A=1.00C=0.00, G=0.00
Latin American 1 Sub222A=0.968C=0.032, G=0.000
Latin American 2 Sub1176A=0.9558C=0.0442, G=0.0000
South Asian Sub4918A=0.8015C=0.1985, G=0.0000

There is also the uncommon MET variant:
View attachment 598618

View attachment 598617

PopulationGroupSample SizeRef AlleleAlt Allele

PopulationGroupSample SizeRef AlleleAlt Allele
Total Global18518C=0.57436G=0.42564
European Sub14150C=0.54580G=0.45420
African Sub2898C=0.7502G=0.2498
African Others Sub114C=0.798G=0.202
African American Sub2784C=0.7482G=0.2518
Asian Sub112C=0.384G=0.616
East Asian Sub86C=0.36G=0.64


tl;dr

what are the conclusions of this study?
 

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