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rs72558112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558112(C;G)
Make rs72558112(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356401
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558112
ebirs72558112
HLIrs72558112
Exacrs72558112
Varsomers72558112
Maprs72558112
PheGenIrs72558112
hapmaprs72558112
1000 genomesrs72558112
hgdprs72558112
ensemblrs72558112
gopubmedrs72558112
geneviewrs72558112
scholarrs72558112
googlers72558112
pharmgkbrs72558112
gwascentralrs72558112
openSNPrs72558112
23andMers72558112
23andMe allrs72558112
SNP Nexus

SNPshotrs72558112
SNPdbers72558112
MSV3drs72558112
GWAS Ctlgrs72558112
Max Magnitude0
ClinVar
Risk rs72558112(G,T;G,T)
Alt rs72558112(G,T;G,T)
Reference rs72558112(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324178G>A; NC_000006.11:g.31324178G>C
CLNSRC
CLNACC