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rs1057521062

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521062(C;T)
Make rs1057521062(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71110283
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1057521062
dbSNP (classic)rs1057521062
ClinGenrs1057521062
ebirs1057521062
HLIrs1057521062
Exacrs1057521062
Gnomadrs1057521062
Varsomers1057521062
LitVarrs1057521062
Maprs1057521062
PheGenIrs1057521062
Biobankrs1057521062
1000 genomesrs1057521062
hgdprs1057521062
ensemblrs1057521062
geneviewrs1057521062
scholarrs1057521062
googlers1057521062
pharmgkbrs1057521062
gwascentralrs1057521062
openSNPrs1057521062
23andMers1057521062
23andMe allrs1057521062
SNPshotrs1057521062
SNPdbers1057521062
MSV3drs1057521062
GWAS Ctlgrs1057521062
Max Magnitude0
ClinVar
Risk rs1057521062(T;T)
Alt rs1057521062(T;T)
Reference Rs1057521062(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70330133G>A
CLNSRC
CLNACC RCV000435698.1,