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rs72558111

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558111(A;G)
Make rs72558111(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356436
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558111
ebirs72558111
HLIrs72558111
Exacrs72558111
Varsomers72558111
Maprs72558111
PheGenIrs72558111
hapmaprs72558111
1000 genomesrs72558111
hgdprs72558111
ensemblrs72558111
gopubmedrs72558111
geneviewrs72558111
scholarrs72558111
googlers72558111
pharmgkbrs72558111
gwascentralrs72558111
openSNPrs72558111
23andMers72558111
23andMe allrs72558111
SNP Nexus

SNPshotrs72558111
SNPdbers72558111
MSV3drs72558111
GWAS Ctlgrs72558111
Max Magnitude0
ClinVar
Risk rs72558111(C,G;C,G)
Alt rs72558111(C,G;C,G)
Reference rs72558111(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324213T>C; NC_000006.11:g.31324213T>G
CLNSRC
CLNACC