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rs45610732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45610732(A;G)
Make rs45610732(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position31355577
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs45610732
dbSNP (old)rs45610732
ClinGenrs45610732
ebirs45610732
HLIrs45610732
Exacrs45610732
Gnomadrs45610732
Varsomers45610732
Maprs45610732
PheGenIrs45610732
Biobankrs45610732
1000 genomesrs45610732
hgdprs45610732
ensemblrs45610732
gopubmedrs45610732
geneviewrs45610732
scholarrs45610732
googlers45610732
pharmgkbrs45610732
gwascentralrs45610732
openSNPrs45610732
23andMers45610732
23andMe allrs45610732
SNP Nexus

SNPshotrs45610732
SNPdbers45610732
MSV3drs45610732
GWAS Ctlgrs45610732
Max Magnitude0
ClinVar
Risk rs45610732(G;G)
Alt rs45610732(G;G)
Reference Rs45610732(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323354T>C
CLNSRC
CLNACC