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rs121913077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913077(C;T)
Make rs121913077(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014259
GeneFAS
is asnp
is mentioned by
dbSNPrs121913077
ebirs121913077
HLIrs121913077
Exacrs121913077
Varsomers121913077
Maprs121913077
PheGenIrs121913077
hapmaprs121913077
1000 genomesrs121913077
hgdprs121913077
ensemblrs121913077
gopubmedrs121913077
geneviewrs121913077
scholarrs121913077
googlers121913077
pharmgkbrs121913077
gwascentralrs121913077
openSNPrs121913077
23andMers121913077
23andMe allrs121913077
SNP Nexus

SNPshotrs121913077
SNPdbers121913077
MSV3drs121913077
GWAS Ctlgrs121913077
Max Magnitude0
OMIM134637
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913077(T;T)
Alt rs121913077(T;T)
Reference rs121913077(C;C)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90774016C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017965.29,