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rs151341206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341206(A;G)
Make rs151341206(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356699
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341206
dbSNP (classic)rs151341206
ClinGenrs151341206
ebirs151341206
HLIrs151341206
Exacrs151341206
Gnomadrs151341206
Varsomers151341206
LitVarrs151341206
Maprs151341206
PheGenIrs151341206
Biobankrs151341206
1000 genomesrs151341206
hgdprs151341206
ensemblrs151341206
geneviewrs151341206
scholarrs151341206
googlers151341206
pharmgkbrs151341206
gwascentralrs151341206
openSNPrs151341206
23andMers151341206
SNPshotrs151341206
SNPdbers151341206
MSV3drs151341206
GWAS Ctlgrs151341206
Max Magnitude0
ClinVar
Risk rs151341206(G;G)
Alt rs151341206(G;G)
Reference Rs151341206(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324476T>C
CLNSRC
CLNACC