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rs72558157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558157(C;C)
Make rs72558157(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269794
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558157
ebirs72558157
HLIrs72558157
Exacrs72558157
Varsomers72558157
Maprs72558157
PheGenIrs72558157
hapmaprs72558157
1000 genomesrs72558157
hgdprs72558157
ensemblrs72558157
gopubmedrs72558157
geneviewrs72558157
scholarrs72558157
googlers72558157
pharmgkbrs72558157
gwascentralrs72558157
openSNPrs72558157
23andMers72558157
23andMe allrs72558157
SNP Nexus

SNPshotrs72558157
SNPdbers72558157
MSV3drs72558157
GWAS Ctlgrs72558157
Max Magnitude0
ClinVar
Risk rs72558157(C;C)
Alt rs72558157(C;C)
Reference rs72558157(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237571A>G
CLNSRC
CLNACC