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rs72558110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558110(C;T)
Make rs72558110(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356724
GeneHLA-B
is asnp
is mentioned by
dbSNPrs72558110
ebirs72558110
HLIrs72558110
Exacrs72558110
Varsomers72558110
Maprs72558110
PheGenIrs72558110
hapmaprs72558110
1000 genomesrs72558110
hgdprs72558110
ensemblrs72558110
gopubmedrs72558110
geneviewrs72558110
scholarrs72558110
googlers72558110
pharmgkbrs72558110
gwascentralrs72558110
openSNPrs72558110
23andMers72558110
23andMe allrs72558110
SNP Nexus

SNPshotrs72558110
SNPdbers72558110
MSV3drs72558110
GWAS Ctlgrs72558110
Max Magnitude0
ClinVar
Risk rs72558110(A,G,T;A,G,T)
Alt rs72558110(A,G,T;A,G,T)
Reference rs72558110(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324501G>A; NC_000006.11:g.31324501G>T
CLNSRC
CLNACC