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rs1057517950

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517950(C;C)
Make rs1057517950(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71109267
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1057517950
dbSNP (old)rs1057517950
ClinGenrs1057517950
ebirs1057517950
HLIrs1057517950
Exacrs1057517950
Gnomadrs1057517950
Varsomers1057517950
Maprs1057517950
PheGenIrs1057517950
Biobankrs1057517950
1000 genomesrs1057517950
hgdprs1057517950
ensemblrs1057517950
gopubmedrs1057517950
geneviewrs1057517950
scholarrs1057517950
googlers1057517950
pharmgkbrs1057517950
gwascentralrs1057517950
openSNPrs1057517950
23andMers1057517950
23andMe allrs1057517950
SNPshotrs1057517950
SNPdbers1057517950
MSV3drs1057517950
GWAS Ctlgrs1057517950
Max Magnitude0
ClinVar
Risk rs1057517950(C;C)
Alt rs1057517950(C;C)
Reference Rs1057517950(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70329117A>G
CLNSRC
CLNACC RCV000413285.1,