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rs137854682

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854682(C;G)
Make rs137854682(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356737
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs137854682
dbSNP (old)rs137854682
ClinGenrs137854682
ebirs137854682
HLIrs137854682
Exacrs137854682
Varsomers137854682
Maprs137854682
PheGenIrs137854682
Biobankrs137854682
1000 genomesrs137854682
hgdprs137854682
ensemblrs137854682
gopubmedrs137854682
geneviewrs137854682
scholarrs137854682
googlers137854682
pharmgkbrs137854682
gwascentralrs137854682
openSNPrs137854682
23andMers137854682
23andMe allrs137854682
SNP Nexus

SNPshotrs137854682
SNPdbers137854682
MSV3drs137854682
GWAS Ctlgrs137854682
Max Magnitude0
ClinVar
Risk rs137854682(G;G) rs137854682(T;T)
Alt rs137854682(G;G) rs137854682(T;T)
Reference Rs137854682(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324514G>A; NC_000006.11:g.31324514G>C
CLNSRC
CLNACC