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rs121913080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913080(C;C)
Make rs121913080(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014191
GeneFAS
is asnp
is mentioned by
dbSNPrs121913080
ebirs121913080
HLIrs121913080
Exacrs121913080
Varsomers121913080
Maprs121913080
PheGenIrs121913080
hapmaprs121913080
1000 genomesrs121913080
hgdprs121913080
ensemblrs121913080
gopubmedrs121913080
geneviewrs121913080
scholarrs121913080
googlers121913080
pharmgkbrs121913080
gwascentralrs121913080
openSNPrs121913080
23andMers121913080
23andMe allrs121913080
SNP Nexus

SNPshotrs121913080
SNPdbers121913080
MSV3drs121913080
GWAS Ctlgrs121913080
Max Magnitude0
OMIM134637
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913080(C;C)
Alt rs121913080(C;C)
Reference rs121913080(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.90773948G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017969.29,