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rs121913079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913079(A;G)
Make rs121913079(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014137
GeneFAS
is asnp
is mentioned by
dbSNPrs121913079
ebirs121913079
HLIrs121913079
Exacrs121913079
Varsomers121913079
Maprs121913079
PheGenIrs121913079
hapmaprs121913079
1000 genomesrs121913079
hgdprs121913079
ensemblrs121913079
gopubmedrs121913079
geneviewrs121913079
scholarrs121913079
googlers121913079
pharmgkbrs121913079
gwascentralrs121913079
openSNPrs121913079
23andMers121913079
23andMe allrs121913079
SNP Nexus

SNPshotrs121913079
SNPdbers121913079
MSV3drs121913079
GWAS Ctlgrs121913079
Max Magnitude0
OMIM134637
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121913079(G;G)
Alt rs121913079(G;G)
Reference rs121913079(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.90773894A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017967.29,