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rs12526858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs12526858(C;C)
Make rs12526858(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355944
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs12526858
dbSNP (classic)rs12526858
ClinGenrs12526858
ebirs12526858
HLIrs12526858
Exacrs12526858
Gnomadrs12526858
Varsomers12526858
LitVarrs12526858
Maprs12526858
PheGenIrs12526858
Biobankrs12526858
1000 genomesrs12526858
hgdprs12526858
ensemblrs12526858
geneviewrs12526858
scholarrs12526858
googlers12526858
pharmgkbrs12526858
gwascentralrs12526858
openSNPrs12526858
23andMers12526858
SNPshotrs12526858
SNPdbers12526858
MSV3drs12526858
GWAS Ctlgrs12526858
GMAF0.1226
Max Magnitude0
ClinVar
Risk rs12526858(C;C)
Alt rs12526858(C;C)
Reference Rs12526858(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323721G>C
CLNSRC
CLNACC