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rs121913086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913086(G;T)
Make rs121913086(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89014220
GeneFAS
is asnp
is mentioned by
dbSNPrs121913086
ebirs121913086
HLIrs121913086
Exacrs121913086
Varsomers121913086
Maprs121913086
PheGenIrs121913086
hapmaprs121913086
1000 genomesrs121913086
hgdprs121913086
ensemblrs121913086
gopubmedrs121913086
geneviewrs121913086
scholarrs121913086
googlers121913086
pharmgkbrs121913086
gwascentralrs121913086
openSNPrs121913086
23andMers121913086
23andMe allrs121913086
SNP Nexus

SNPshotrs121913086
SNPdbers121913086
MSV3drs121913086
GWAS Ctlgrs121913086
Max Magnitude0
OMIM134637
Desc
Variant0020
Relatedalso
ClinVar
Risk rs121913086(T;T)
Alt rs121913086(T;T)
Reference rs121913086(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.90773977G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017980.29,