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rs121913082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913082(A;G)
Make rs121913082(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014205
GeneFAS
is asnp
is mentioned by
dbSNPrs121913082
ebirs121913082
HLIrs121913082
Exacrs121913082
Varsomers121913082
Maprs121913082
PheGenIrs121913082
hapmaprs121913082
1000 genomesrs121913082
hgdprs121913082
ensemblrs121913082
gopubmedrs121913082
geneviewrs121913082
scholarrs121913082
googlers121913082
pharmgkbrs121913082
gwascentralrs121913082
openSNPrs121913082
23andMers121913082
23andMe allrs121913082
SNP Nexus

SNPshotrs121913082
SNPdbers121913082
MSV3drs121913082
GWAS Ctlgrs121913082
Max Magnitude0
OMIM134637
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121913082(G;G)
Alt rs121913082(G;G)
Reference rs121913082(A;A)
Significance Pathogenic
Disease SQUAMOUS CELL CARCINOMA
Variation info
Gene FAS
CLNDBN SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
Reversed 0
HGVS NC_000010.10:g.90773962A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017974.5,