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rs72558119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558119(C;T)
Make rs72558119(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356210
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558119
ebirs72558119
HLIrs72558119
Exacrs72558119
Varsomers72558119
Maprs72558119
PheGenIrs72558119
hapmaprs72558119
1000 genomesrs72558119
hgdprs72558119
ensemblrs72558119
gopubmedrs72558119
geneviewrs72558119
scholarrs72558119
googlers72558119
pharmgkbrs72558119
gwascentralrs72558119
openSNPrs72558119
23andMers72558119
23andMe allrs72558119
SNP Nexus

SNPshotrs72558119
SNPdbers72558119
MSV3drs72558119
GWAS Ctlgrs72558119
Max Magnitude0
ClinVar
Risk rs72558119(T;T)
Alt rs72558119(T;T)
Reference rs72558119(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323987G>A
CLNSRC
CLNACC