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rs151341232

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341232(-;-)
Make rs151341232(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356382
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341232
dbSNP (classic)rs151341232
ClinGenrs151341232
ebirs151341232
HLIrs151341232
Exacrs151341232
Gnomadrs151341232
Varsomers151341232
LitVarrs151341232
Maprs151341232
PheGenIrs151341232
Biobankrs151341232
1000 genomesrs151341232
hgdprs151341232
ensemblrs151341232
geneviewrs151341232
scholarrs151341232
googlers151341232
pharmgkbrs151341232
gwascentralrs151341232
openSNPrs151341232
23andMers151341232
SNPshotrs151341232
SNPdbers151341232
MSV3drs151341232
GWAS Ctlgrs151341232
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341232(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324159delC
CLNSRC
CLNACC