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rs45550032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45550032(C;T)
Make rs45550032(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356901
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45550032
ebirs45550032
HLIrs45550032
Exacrs45550032
Varsomers45550032
Maprs45550032
PheGenIrs45550032
hapmaprs45550032
1000 genomesrs45550032
hgdprs45550032
ensemblrs45550032
gopubmedrs45550032
geneviewrs45550032
scholarrs45550032
googlers45550032
pharmgkbrs45550032
gwascentralrs45550032
openSNPrs45550032
23andMers45550032
23andMe allrs45550032
SNP Nexus

SNPshotrs45550032
SNPdbers45550032
MSV3drs45550032
GWAS Ctlgrs45550032
Max Magnitude0
ClinVar
Risk rs45550032(T;T)
Alt rs45550032(T;T)
Reference rs45550032(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324678G>A
CLNSRC
CLNACC