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rs121913083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913083(A;G)
Make rs121913083(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position89008907
GeneFAS
is asnp
is mentioned by
dbSNPrs121913083
dbSNP (old)rs121913083
ClinGenrs121913083
ebirs121913083
HLIrs121913083
Exacrs121913083
Varsomers121913083
Maprs121913083
PheGenIrs121913083
Biobankrs121913083
1000 genomesrs121913083
hgdprs121913083
ensemblrs121913083
gopubmedrs121913083
geneviewrs121913083
scholarrs121913083
googlers121913083
pharmgkbrs121913083
gwascentralrs121913083
openSNPrs121913083
23andMers121913083
23andMe allrs121913083
SNP Nexus

SNPshotrs121913083
SNPdbers121913083
MSV3drs121913083
GWAS Ctlgrs121913083
Max Magnitude0
OMIM134637
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121913083(G;G)
Alt rs121913083(G;G)
Reference Rs121913083(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.90768664A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017975.5,