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

rs1057517747

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517747(C;T)
Make rs1057517747(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71111497
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1057517747
dbSNP (old)rs1057517747
ClinGenrs1057517747
ebirs1057517747
HLIrs1057517747
Exacrs1057517747
Gnomadrs1057517747
Varsomers1057517747
LitVarrs1057517747
Maprs1057517747
PheGenIrs1057517747
Biobankrs1057517747
1000 genomesrs1057517747
hgdprs1057517747
ensemblrs1057517747
gopubmedrs1057517747
geneviewrs1057517747
scholarrs1057517747
googlers1057517747
pharmgkbrs1057517747
gwascentralrs1057517747
openSNPrs1057517747
23andMers1057517747
23andMe allrs1057517747
SNPshotrs1057517747
SNPdbers1057517747
MSV3drs1057517747
GWAS Ctlgrs1057517747
Max Magnitude0
ClinVar
Risk rs1057517747(T;T)
Alt rs1057517747(T;T)
Reference Rs1057517747(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70331347G>A
CLNSRC
CLNACC RCV000412822.1,