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rs1064793153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position71110290
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1064793153
dbSNP (old)rs1064793153
ClinGenrs1064793153
ebirs1064793153
HLIrs1064793153
Exacrs1064793153
Gnomadrs1064793153
Varsomers1064793153
LitVarrs1064793153
Maprs1064793153
PheGenIrs1064793153
Biobankrs1064793153
1000 genomesrs1064793153
hgdprs1064793153
ensemblrs1064793153
gopubmedrs1064793153
geneviewrs1064793153
scholarrs1064793153
googlers1064793153
pharmgkbrs1064793153
gwascentralrs1064793153
openSNPrs1064793153
23andMers1064793153
23andMe allrs1064793153
SNPshotrs1064793153
SNPdbers1064793153
MSV3drs1064793153
GWAS Ctlgrs1064793153
Max Magnitude0
ClinVar
Risk rs1064793153(T;T)
Alt rs1064793153(T;T)
Reference Rs1064793153(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70330140G>A
CLNSRC
CLNACC RCV000480139.1,