@Nopish
@Nopish
Yeah, that's what I am worried about, but I might find a good one. I still risk sending my DNA to the Jews though.
its not a scam its just highly inaccurate
I
True
You would think so, wouldn't you?
Observe:
"My doctors don't know why my cholesterol is so high!" - Mother
I've had 30X whole genome sequencing. Mother has been genotyped.
Table 2. Individual FH Variants (≥30 carriers) Associated With Elevated maxLDL-C Among 331 107 Multiethnic Veterans
Mother:
Myself:
www.ncbi.nlm.nih.gov
Indeed. Mother has the illness while I am carrier for a very rare variant of it. The test was almost certainly accurate.
Observe:
"My doctors don't know why my cholesterol is so high!" - Mother
I've had 30X whole genome sequencing. Mother has been genotyped.
Table 2. Individual FH Variants (≥30 carriers) Associated With Elevated maxLDL-C Among 331 107 Multiethnic Veterans
SNP ID | Chr: Basepair Position | Gene | Effective Allele | Amino Acid Substitution | No.of Carriers | Beta±SE | P Value | maxLDL≥190 (%) |
|---|---|---|---|---|---|---|---|---|
rs141502002 | 1:55524222 | PCSK9 | T | Arg469Trp | 1147 | 9.4±1.1 | 3.71×10–17 | 17.9 |
rs12713559 | 2:21229068 | APOB | A | Arg3558Cys | 366 | 9.9±2.0 | 6.32×10–7 | 15.3 |
rs5742904 | 2:21229160 | APOB | T | Arg3527Gln | 256 | 43.5±2.4 | 3.40×10–75 | 42.2 |
rs768563000 | 19:11217264 | LDLR | A | Glu240Ter | 34 | 20.3±6.5 | 1.8×10–3 | 26.5 |
rs151207122 | 19:11218157 | LDLR | T | Arg303Trp | 49 | 36.2±5.4 | 2.16×10–11 | 36.7 |
rs121908030 | 19:11218160 | LDLR | A | Asp304Tyr | 30 | 80.2±6.9 | 4.67×10–31 | 66.7 |
rs201573863 | 19:11231154 | LDLR | T | Pro699Leu | 51 | 44.0±5.3 | 1.03×10–16 | 51.0 |
rs137853964 | 19:11240278 | LDLR | A | Val827Ile | 328 | 12.6±2.1 | 1.67×10–9 | 18.0 |
Effects of Genetic Variants Associated with Familial Hypercholesterolemia on Low-Density Lipoprotein-Cholesterol Levels and Cardiovascular Outcomes in the Million Veteran Program
Background: Familial hypercholesterolemia (FH) is characterized by inherited high levels of LDL-C (low-density lipoprotein cholesterol) and premature coronary heart disease. Over a thousand low-frequ
www.ahajournals.org
Mother:
Myself:
| Population | Group | Sample Size | Ref Allele | Alt |
|---|
| Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|
| Total | Global | 199288 | C=0.999729 | T=0.000271 |
| European | Sub | 169946 | C=0.999953 | T=0.000047 |
| African | Sub | 4954 | C=0.9923 | T=0.0077 |
| African Others | Sub | 176 | C=1.000 | T=0.000 |
| African American | Sub | 4778 | C=0.9920 | T=0.0080 |
| Asian | Sub | 6350 | C=0.9998 | T=0.0002 |
| East Asian | Sub | 4502 | C=0.9998 | T=0.0002 |
rs141502002 RefSNP Report - dbSNP - NCBI
www.ncbi.nlm.nih.gov
Indeed. Mother has the illness while I am carrier for a very rare variant of it. The test was almost certainly accurate.
C
Can you teach me how to read thatYou would think so, wouldn't you?
Observe:
"My doctors don't know why my cholesterol is so high!" - Mother
I've had 30X whole genome sequencing. Mother has been genotyped.
Table 2. Individual FH Variants (≥30 carriers) Associated With Elevated maxLDL-C Among 331 107 Multiethnic Veterans
Effects of Genetic Variants Associated with Familial Hypercholesterolemia on Low-Density Lipoprotein-Cholesterol Levels and Cardiovascular Outcomes in the Million Veteran Program
Background: Familial hypercholesterolemia (FH) is characterized by inherited high levels of LDL-C (low-density lipoprotein cholesterol) and premature coronary heart disease. Over a thousand low-frequwww.ahajournals.org
Mother:
View attachment 597297
View attachment 597298
Myself:
View attachment 597299
Population Group Sample Size Ref Allele Alt
Population Group Sample Size Ref Allele Alt Allele Total Global 199288 C=0.999729 T=0.000271 European Sub 169946 C=0.999953 T=0.000047 African Sub 4954 C=0.9923 T=0.0077 African Others Sub 176 C=1.000 T=0.000 African American Sub 4778 C=0.9920 T=0.0080 Asian Sub 6350 C=0.9998 T=0.0002 East Asian Sub 4502 C=0.9998 T=0.0002
rs141502002 RefSNP Report - dbSNP - NCBI
Indeed. Mother has the illness while I am carrier for a very rare variant of it. The test was almost certainly accurate.
Similar threads
Users who are viewing this thread
