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rs1064793338

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position71110630
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1064793338
dbSNP (old)rs1064793338
ClinGenrs1064793338
ebirs1064793338
HLIrs1064793338
Exacrs1064793338
Gnomadrs1064793338
Varsomers1064793338
Maprs1064793338
PheGenIrs1064793338
Biobankrs1064793338
1000 genomesrs1064793338
hgdprs1064793338
ensemblrs1064793338
gopubmedrs1064793338
geneviewrs1064793338
scholarrs1064793338
googlers1064793338
pharmgkbrs1064793338
gwascentralrs1064793338
openSNPrs1064793338
23andMers1064793338
23andMe allrs1064793338
SNPshotrs1064793338
SNPdbers1064793338
MSV3drs1064793338
GWAS Ctlgrs1064793338
Max Magnitude0
ClinVar
Risk rs1064793338(-;-)
Alt rs1064793338(-;-)
Reference Rs1064793338(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70330480delC
CLNSRC
CLNACC RCV000482132.1,