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rs151341111

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341111(A;A)
Make rs151341111(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356863
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341111
dbSNP (classic)rs151341111
ClinGenrs151341111
ebirs151341111
HLIrs151341111
Exacrs151341111
Gnomadrs151341111
Varsomers151341111
LitVarrs151341111
Maprs151341111
PheGenIrs151341111
Biobankrs151341111
1000 genomesrs151341111
hgdprs151341111
ensemblrs151341111
geneviewrs151341111
scholarrs151341111
googlers151341111
pharmgkbrs151341111
gwascentralrs151341111
openSNPrs151341111
23andMers151341111
SNPshotrs151341111
SNPdbers151341111
MSV3drs151341111
GWAS Ctlgrs151341111
Max Magnitude0
ClinVar
Risk rs151341111(A;A)
Alt rs151341111(A;A)
Reference Rs151341111(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324640C>T
CLNSRC
CLNACC