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rs121913084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913084(C;C)
Make rs121913084(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89010779
GeneFAS
is asnp
is mentioned by
dbSNPrs121913084
ebirs121913084
HLIrs121913084
Exacrs121913084
Varsomers121913084
Maprs121913084
PheGenIrs121913084
hapmaprs121913084
1000 genomesrs121913084
hgdprs121913084
ensemblrs121913084
gopubmedrs121913084
geneviewrs121913084
scholarrs121913084
googlers121913084
pharmgkbrs121913084
gwascentralrs121913084
openSNPrs121913084
23andMers121913084
23andMe allrs121913084
SNP Nexus

SNPshotrs121913084
SNPdbers121913084
MSV3drs121913084
GWAS Ctlgrs121913084
Max Magnitude0
OMIM134637
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121913084(C;C)
Alt rs121913084(C;C)
Reference rs121913084(T;T)
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.90770536T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017976.5,