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rs151341200

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341200(A;G)
Make rs151341200(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356705
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341200
dbSNP (classic)rs151341200
ClinGenrs151341200
ebirs151341200
HLIrs151341200
Exacrs151341200
Gnomadrs151341200
Varsomers151341200
LitVarrs151341200
Maprs151341200
PheGenIrs151341200
Biobankrs151341200
1000 genomesrs151341200
hgdprs151341200
ensemblrs151341200
geneviewrs151341200
scholarrs151341200
googlers151341200
pharmgkbrs151341200
gwascentralrs151341200
openSNPrs151341200
23andMers151341200
SNPshotrs151341200
SNPdbers151341200
MSV3drs151341200
GWAS Ctlgrs151341200
Max Magnitude0
ClinVar
Risk rs151341200(G;G)
Alt rs151341200(G;G)
Reference Rs151341200(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324482T>C
CLNSRC
CLNACC