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rs151341315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341315(A;C)
Make rs151341315(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356232
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341315
dbSNP (classic)rs151341315
ClinGenrs151341315
ebirs151341315
HLIrs151341315
Exacrs151341315
Gnomadrs151341315
Varsomers151341315
LitVarrs151341315
Maprs151341315
PheGenIrs151341315
Biobankrs151341315
1000 genomesrs151341315
hgdprs151341315
ensemblrs151341315
geneviewrs151341315
scholarrs151341315
googlers151341315
pharmgkbrs151341315
gwascentralrs151341315
openSNPrs151341315
23andMers151341315
SNPshotrs151341315
SNPdbers151341315
MSV3drs151341315
GWAS Ctlgrs151341315
Max Magnitude0
ClinVar
Risk rs151341315(C;C)
Alt rs151341315(C;C)
Reference Rs151341315(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324009T>G
CLNSRC
CLNACC