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

rs137852510

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852510(A;A)
Make rs137852510(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position71108323
GeneCXorf65, IL2RG
is asnp
is mentioned by
dbSNPrs137852510
ebirs137852510
HLIrs137852510
Exacrs137852510
Varsomers137852510
Maprs137852510
PheGenIrs137852510
hapmaprs137852510
1000 genomesrs137852510
hgdprs137852510
ensemblrs137852510
gopubmedrs137852510
geneviewrs137852510
scholarrs137852510
googlers137852510
pharmgkbrs137852510
gwascentralrs137852510
openSNPrs137852510
23andMers137852510
23andMe allrs137852510
SNP Nexus

SNPshotrs137852510
SNPdbers137852510
MSV3drs137852510
GWAS Ctlgrs137852510
Max Magnitude0
OMIM308380
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137852510(A;A)
Alt rs137852510(A;A)
Reference rs137852510(T;T)
Significance Pathogenic
Disease Combined immunodeficiency
Variation info
Gene CXorf65 IL2RG
CLNDBN Combined immunodeficiency, X-linked
Reversed 1
HGVS NC_000023.10:g.70328173A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010706.3,