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rs45627838

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45627838(G;T)
Make rs45627838(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357079
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45627838
ebirs45627838
HLIrs45627838
Exacrs45627838
Varsomers45627838
Maprs45627838
PheGenIrs45627838
hapmaprs45627838
1000 genomesrs45627838
hgdprs45627838
ensemblrs45627838
gopubmedrs45627838
geneviewrs45627838
scholarrs45627838
googlers45627838
pharmgkbrs45627838
gwascentralrs45627838
openSNPrs45627838
23andMers45627838
23andMe allrs45627838
SNP Nexus

SNPshotrs45627838
SNPdbers45627838
MSV3drs45627838
GWAS Ctlgrs45627838
Max Magnitude0
ClinVar
Risk rs45627838(T;T)
Alt rs45627838(T;T)
Reference rs45627838(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324856C>A
CLNSRC
CLNACC