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rs151341106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341106(A;G)
Make rs151341106(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356892
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341106
dbSNP (classic)rs151341106
ClinGenrs151341106
ebirs151341106
HLIrs151341106
Exacrs151341106
Gnomadrs151341106
Varsomers151341106
LitVarrs151341106
Maprs151341106
PheGenIrs151341106
Biobankrs151341106
1000 genomesrs151341106
hgdprs151341106
ensemblrs151341106
geneviewrs151341106
scholarrs151341106
googlers151341106
pharmgkbrs151341106
gwascentralrs151341106
openSNPrs151341106
23andMers151341106
SNPshotrs151341106
SNPdbers151341106
MSV3drs151341106
GWAS Ctlgrs151341106
Max Magnitude0
ClinVar
Risk rs151341106(G;G)
Alt rs151341106(G;G)
Reference Rs151341106(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324669T>C
CLNSRC
CLNACC