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rs45512291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45512291(A;A)
Make rs45512291(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356828
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45512291
ebirs45512291
HLIrs45512291
Exacrs45512291
Varsomers45512291
Maprs45512291
PheGenIrs45512291
hapmaprs45512291
1000 genomesrs45512291
hgdprs45512291
ensemblrs45512291
gopubmedrs45512291
geneviewrs45512291
scholarrs45512291
googlers45512291
pharmgkbrs45512291
gwascentralrs45512291
openSNPrs45512291
23andMers45512291
23andMe allrs45512291
SNP Nexus

SNPshotrs45512291
SNPdbers45512291
MSV3drs45512291
GWAS Ctlgrs45512291
Max Magnitude0
ClinVar
Risk rs45512291(A,C;A,C)
Alt rs45512291(A,C;A,C)
Reference rs45512291(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324605C>G; NC_000006.11:g.31324605C>T
CLNSRC
CLNACC