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rs7901656

From SNPedia

Orientationplus
Stabilizedplus
Make rs7901656(C;C)
Make rs7901656(C;T)
Make rs7901656(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position89006456
GeneFAS
is asnp
is mentioned by
dbSNPrs7901656
ebirs7901656
HLIrs7901656
Exacrs7901656
Varsomers7901656
Maprs7901656
PheGenIrs7901656
hapmaprs7901656
1000 genomesrs7901656
hgdprs7901656
ensemblrs7901656
gopubmedrs7901656
geneviewrs7901656
scholarrs7901656
googlers7901656
pharmgkbrs7901656
gwascentralrs7901656
openSNPrs7901656
23andMers7901656
23andMe allrs7901656
SNP Nexus

SNPshotrs7901656
SNPdbers7901656
MSV3drs7901656
GWAS Ctlgrs7901656
GMAF0.3476
Max Magnitude
? (C;C) (C;T) (T;T) 28

[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