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rs45539837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45539837(G;G)
Make rs45539837(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357080
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45539837
ebirs45539837
HLIrs45539837
Exacrs45539837
Varsomers45539837
Maprs45539837
PheGenIrs45539837
hapmaprs45539837
1000 genomesrs45539837
hgdprs45539837
ensemblrs45539837
gopubmedrs45539837
geneviewrs45539837
scholarrs45539837
googlers45539837
pharmgkbrs45539837
gwascentralrs45539837
openSNPrs45539837
23andMers45539837
23andMe allrs45539837
SNP Nexus

SNPshotrs45539837
SNPdbers45539837
MSV3drs45539837
GWAS Ctlgrs45539837
Max Magnitude0
ClinVar
Risk rs45539837(G;G)
Alt rs45539837(G;G)
Reference rs45539837(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324857A>C
CLNSRC
CLNACC