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rs121913081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913081(C;T)
Make rs121913081(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014251
GeneFAS
is asnp
is mentioned by
dbSNPrs121913081
ebirs121913081
HLIrs121913081
Exacrs121913081
Varsomers121913081
Maprs121913081
PheGenIrs121913081
hapmaprs121913081
1000 genomesrs121913081
hgdprs121913081
ensemblrs121913081
gopubmedrs121913081
geneviewrs121913081
scholarrs121913081
googlers121913081
pharmgkbrs121913081
gwascentralrs121913081
openSNPrs121913081
23andMers121913081
23andMe allrs121913081
SNP Nexus

SNPshotrs121913081
SNPdbers121913081
MSV3drs121913081
GWAS Ctlgrs121913081
Max Magnitude0
OMIM134637
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121913081(T;T)
Alt rs121913081(T;T)
Reference rs121913081(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.90774008C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017970.29,