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rs151341163

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341163(-;-)
Make rs151341163(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356780
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341163
dbSNP (classic)rs151341163
ClinGenrs151341163
ebirs151341163
HLIrs151341163
Exacrs151341163
Gnomadrs151341163
Varsomers151341163
LitVarrs151341163
Maprs151341163
PheGenIrs151341163
Biobankrs151341163
1000 genomesrs151341163
hgdprs151341163
ensemblrs151341163
geneviewrs151341163
scholarrs151341163
googlers151341163
pharmgkbrs151341163
gwascentralrs151341163
openSNPrs151341163
23andMers151341163
SNPshotrs151341163
SNPdbers151341163
MSV3drs151341163
GWAS Ctlgrs151341163
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341163(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324557delC
CLNSRC
CLNACC