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rs151341354

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341354(A;A)
Make rs151341354(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355399
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341354
dbSNP (classic)rs151341354
ClinGenrs151341354
ebirs151341354
HLIrs151341354
Exacrs151341354
Gnomadrs151341354
Varsomers151341354
LitVarrs151341354
Maprs151341354
PheGenIrs151341354
Biobankrs151341354
1000 genomesrs151341354
hgdprs151341354
ensemblrs151341354
geneviewrs151341354
scholarrs151341354
googlers151341354
pharmgkbrs151341354
gwascentralrs151341354
openSNPrs151341354
23andMers151341354
SNPshotrs151341354
SNPdbers151341354
MSV3drs151341354
GWAS Ctlgrs151341354
Max Magnitude0
ClinVar
Risk rs151341354(A;A)
Alt rs151341354(A;A)
Reference Rs151341354(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323176C>T
CLNSRC
CLNACC