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rs121913085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913085(C;C)
Make rs121913085(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014182
GeneFAS
is asnp
is mentioned by
dbSNPrs121913085
ebirs121913085
HLIrs121913085
Exacrs121913085
Varsomers121913085
Maprs121913085
PheGenIrs121913085
hapmaprs121913085
1000 genomesrs121913085
hgdprs121913085
ensemblrs121913085
gopubmedrs121913085
geneviewrs121913085
scholarrs121913085
googlers121913085
pharmgkbrs121913085
gwascentralrs121913085
openSNPrs121913085
23andMers121913085
23andMe allrs121913085
SNP Nexus

SNPshotrs121913085
SNPdbers121913085
MSV3drs121913085
GWAS Ctlgrs121913085
Merged fromRs28929499
Max Magnitude0
OMIM134637
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121913085(C;C)
Alt rs121913085(C;C)
Reference rs121913085(G;G)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90773939G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017977.29,