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rs45566634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45566634(G;T)
Make rs45566634(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357083
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45566634
ebirs45566634
HLIrs45566634
Exacrs45566634
Varsomers45566634
Maprs45566634
PheGenIrs45566634
hapmaprs45566634
1000 genomesrs45566634
hgdprs45566634
ensemblrs45566634
gopubmedrs45566634
geneviewrs45566634
scholarrs45566634
googlers45566634
pharmgkbrs45566634
gwascentralrs45566634
openSNPrs45566634
23andMers45566634
23andMe allrs45566634
SNP Nexus

SNPshotrs45566634
SNPdbers45566634
MSV3drs45566634
GWAS Ctlgrs45566634
Max Magnitude0
ClinVar
Risk rs45566634(T;T)
Alt rs45566634(T;T)
Reference rs45566634(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324860C>A
CLNSRC
CLNACC