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rs1057520644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520644(A;A)
Make rs1057520644(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71110964
GeneIL2RG
is asnp
is mentioned by
dbSNPrs1057520644
dbSNP (classic)rs1057520644
ClinGenrs1057520644
ebirs1057520644
HLIrs1057520644
Exacrs1057520644
Gnomadrs1057520644
Varsomers1057520644
LitVarrs1057520644
Maprs1057520644
PheGenIrs1057520644
Biobankrs1057520644
1000 genomesrs1057520644
hgdprs1057520644
ensemblrs1057520644
geneviewrs1057520644
scholarrs1057520644
googlers1057520644
pharmgkbrs1057520644
gwascentralrs1057520644
openSNPrs1057520644
23andMers1057520644
23andMe allrs1057520644
SNPshotrs1057520644
SNPdbers1057520644
MSV3drs1057520644
GWAS Ctlgrs1057520644
Max Magnitude0
ClinVar
Risk rs1057520644(A;A)
Alt rs1057520644(A;A)
Reference Rs1057520644(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IL2RG
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.70330814C>T
CLNSRC
CLNACC RCV000427716.1,