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rs104894764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894764(G;T)
Make rs104894764(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position123886014
GeneXIAP
is asnp
is mentioned by
dbSNPrs104894764
ebirs104894764
HLIrs104894764
Exacrs104894764
Varsomers104894764
Maprs104894764
PheGenIrs104894764
hapmaprs104894764
1000 genomesrs104894764
hgdprs104894764
ensemblrs104894764
gopubmedrs104894764
geneviewrs104894764
scholarrs104894764
googlers104894764
pharmgkbrs104894764
gwascentralrs104894764
openSNPrs104894764
23andMers104894764
23andMe allrs104894764
SNP Nexus

SNPshotrs104894764
SNPdbers104894764
MSV3drs104894764
GWAS Ctlgrs104894764
Max Magnitude0
OMIM300079
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894764(T;T)
Alt rs104894764(T;T)
Reference rs104894764(G;G)
Significance Pathogenic
Disease Lymphoproliferative syndrome 2
Variation info
Gene XIAP
CLNDBN Lymphoproliferative syndrome 2, X-linked
Reversed 0
HGVS NC_000023.10:g.123019864G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012412.22,