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rs45607634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45607634(C;C)
Make rs45607634(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357077
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45607634
ebirs45607634
HLIrs45607634
Exacrs45607634
Varsomers45607634
Maprs45607634
PheGenIrs45607634
hapmaprs45607634
1000 genomesrs45607634
hgdprs45607634
ensemblrs45607634
gopubmedrs45607634
geneviewrs45607634
scholarrs45607634
googlers45607634
pharmgkbrs45607634
gwascentralrs45607634
openSNPrs45607634
23andMers45607634
23andMe allrs45607634
SNP Nexus

SNPshotrs45607634
SNPdbers45607634
MSV3drs45607634
GWAS Ctlgrs45607634
Max Magnitude0
ClinVar
Risk rs45607634(C;C)
Alt rs45607634(C;C)
Reference rs45607634(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324854C>G
CLNSRC
CLNACC