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rs796051887

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051887(A;A)
Make rs796051887(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position6021564
GeneIL2RA
is asnp
is mentioned by
dbSNPrs796051887
ebirs796051887
HLIrs796051887
Exacrs796051887
Varsomers796051887
Maprs796051887
PheGenIrs796051887
hapmaprs796051887
1000 genomesrs796051887
hgdprs796051887
ensemblrs796051887
gopubmedrs796051887
geneviewrs796051887
scholarrs796051887
googlers796051887
pharmgkbrs796051887
gwascentralrs796051887
openSNPrs796051887
23andMers796051887
23andMe allrs796051887
SNP Nexus

SNPshotrs796051887
SNPdbers796051887
MSV3drs796051887
GWAS Ctlgrs796051887
Max Magnitude0
ClinVar
Risk rs796051887(A;A)
Alt rs796051887(A;A)
Reference rs796051887(G;G)
Significance Pathogenic
Disease Interleukin 2 receptor
Variation info
Gene IL2RA
CLNDBN Interleukin 2 receptor, alpha, deficiency of
Reversed 1
HGVS NC_000010.10:g.6063527C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000185641.3,