Have questions? Visit https://www.reddit.com/r/SNPedia

rs869320660

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320660(A;A)
Make rs869320660(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71109308
GeneIL2RG
is asnp
is mentioned by
dbSNPrs869320660
ebirs869320660
HLIrs869320660
Exacrs869320660
Varsomers869320660
Maprs869320660
PheGenIrs869320660
hapmaprs869320660
1000 genomesrs869320660
hgdprs869320660
ensemblrs869320660
gopubmedrs869320660
geneviewrs869320660
scholarrs869320660
googlers869320660
pharmgkbrs869320660
gwascentralrs869320660
openSNPrs869320660
23andMers869320660
23andMe allrs869320660
SNP Nexus

SNPshotrs869320660
SNPdbers869320660
MSV3drs869320660
GWAS Ctlgrs869320660
Max Magnitude0
ClinVar
Risk rs869320660(A;A)
Alt rs869320660(A;A)
Reference rs869320660(G;G)
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.70329158C>T
CLNSRC
CLNACC RCV000210841.1,