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rs869320659

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320659(C;T)
Make rs869320659(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71109309
GeneIL2RG
is asnp
is mentioned by
dbSNPrs869320659
ebirs869320659
HLIrs869320659
Exacrs869320659
Varsomers869320659
Maprs869320659
PheGenIrs869320659
hapmaprs869320659
1000 genomesrs869320659
hgdprs869320659
ensemblrs869320659
gopubmedrs869320659
geneviewrs869320659
scholarrs869320659
googlers869320659
pharmgkbrs869320659
gwascentralrs869320659
openSNPrs869320659
23andMers869320659
23andMe allrs869320659
SNP Nexus

SNPshotrs869320659
SNPdbers869320659
MSV3drs869320659
GWAS Ctlgrs869320659
Max Magnitude0
ClinVar
Risk rs869320659(T;T)
Alt rs869320659(T;T)
Reference rs869320659(C;C)
Significance Pathogenic
Disease X-linked severe combined immunodeficiency
Variation info
Gene IL2RG
CLNDBN X-linked severe combined immunodeficiency
Reversed 1
HGVS NC_000023.10:g.70329159G>A
CLNSRC
CLNACC RCV000210834.1,