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rs121913076

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913076(A;C)
Make rs121913076(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014163
GeneFAS
is asnp
is mentioned by
dbSNPrs121913076
ebirs121913076
HLIrs121913076
Exacrs121913076
Varsomers121913076
Maprs121913076
PheGenIrs121913076
hapmaprs121913076
1000 genomesrs121913076
hgdprs121913076
ensemblrs121913076
gopubmedrs121913076
geneviewrs121913076
scholarrs121913076
googlers121913076
pharmgkbrs121913076
gwascentralrs121913076
openSNPrs121913076
23andMers121913076
23andMe allrs121913076
SNP Nexus

SNPshotrs121913076
SNPdbers121913076
MSV3drs121913076
GWAS Ctlgrs121913076
Max Magnitude0
OMIM134637
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913076(C;C)
Alt rs121913076(C;C)
Reference rs121913076(A;A)
Significance Pathogenic
Disease Autoimmune lymphoproliferative syndrome
Variation info
Gene FAS
CLNDBN Autoimmune lymphoproliferative syndrome, type 1a
Reversed 0
HGVS NC_000010.10:g.90773920A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017963.29,