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rs151341248

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341248(A;A)
Make rs151341248(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356315
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341248
dbSNP (classic)rs151341248
ClinGenrs151341248
ebirs151341248
HLIrs151341248
Exacrs151341248
Gnomadrs151341248
Varsomers151341248
LitVarrs151341248
Maprs151341248
PheGenIrs151341248
Biobankrs151341248
1000 genomesrs151341248
hgdprs151341248
ensemblrs151341248
geneviewrs151341248
scholarrs151341248
googlers151341248
pharmgkbrs151341248
gwascentralrs151341248
openSNPrs151341248
23andMers151341248
SNPshotrs151341248
SNPdbers151341248
MSV3drs151341248
GWAS Ctlgrs151341248
Max Magnitude0
ClinVar
Risk rs151341248(A;A)
Alt rs151341248(A;A)
Reference Rs151341248(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324092C>T
CLNSRC
CLNACC