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rs137854636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854636(C;G)
Make rs137854636(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356950
GeneHLA-B
is asnp
is mentioned by
dbSNPrs137854636
ebirs137854636
HLIrs137854636
Exacrs137854636
Varsomers137854636
Maprs137854636
PheGenIrs137854636
hapmaprs137854636
1000 genomesrs137854636
hgdprs137854636
ensemblrs137854636
gopubmedrs137854636
geneviewrs137854636
scholarrs137854636
googlers137854636
pharmgkbrs137854636
gwascentralrs137854636
openSNPrs137854636
23andMers137854636
23andMe allrs137854636
SNP Nexus

SNPshotrs137854636
SNPdbers137854636
MSV3drs137854636
GWAS Ctlgrs137854636
Max Magnitude0
ClinVar
Risk rs137854636(G,T;G,T)
Alt rs137854636(G,T;G,T)
Reference rs137854636(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324727G>A; NC_000006.11:g.31324727G>C
CLNSRC
CLNACC