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rs56173567

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56173567(A;A)
Make rs56173567(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356854
GeneHLA-B
is asnp
is mentioned by
dbSNPrs56173567
ebirs56173567
HLIrs56173567
Exacrs56173567
Varsomers56173567
Maprs56173567
PheGenIrs56173567
hapmaprs56173567
1000 genomesrs56173567
hgdprs56173567
ensemblrs56173567
gopubmedrs56173567
geneviewrs56173567
scholarrs56173567
googlers56173567
pharmgkbrs56173567
gwascentralrs56173567
openSNPrs56173567
23andMers56173567
23andMe allrs56173567
SNP Nexus

SNPshotrs56173567
SNPdbers56173567
MSV3drs56173567
GWAS Ctlgrs56173567
Max Magnitude0
ClinVar
Risk rs56173567(A,T;A,T)
Alt rs56173567(A,T;A,T)
Reference rs56173567(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324631C>A; NC_000006.11:g.31324631C>T
CLNSRC
CLNACC