rs7901656
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7901656(C;C) |
Make rs7901656(C;T) |
Make rs7901656(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 89006456 |
Gene | FAS |
is a | snp |
is | mentioned by |
dbSNP | rs7901656 |
dbSNP (classic) | rs7901656 |
ClinGen | rs7901656 |
ebi | rs7901656 |
HLI | rs7901656 |
Exac | rs7901656 |
Gnomad | rs7901656 |
Varsome | rs7901656 |
LitVar | rs7901656 |
Map | rs7901656 |
PheGenI | rs7901656 |
Biobank | rs7901656 |
1000 genomes | rs7901656 |
hgdp | rs7901656 |
ensembl | rs7901656 |
geneview | rs7901656 |
scholar | rs7901656 |
rs7901656 | |
pharmgkb | rs7901656 |
gwascentral | rs7901656 |
openSNP | rs7901656 |
23andMe | rs7901656 |
SNPshot | rs7901656 |
SNPdbe | rs7901656 |
MSV3d | rs7901656 |
GWAS Ctlg | rs7901656 |
GMAF | 0.3476 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 18685642] this snp modulates cystic fibrosis disease severity
[PMID 23141929] A Controlled Case Study of the Relationship Between Environmental Risk Factors and Apoptotic Gene Polymorphism and Lumbar Disc Herniation