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rs151341331

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341331(A;A)
Make rs151341331(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356186
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341331
dbSNP (classic)rs151341331
ClinGenrs151341331
ebirs151341331
HLIrs151341331
Exacrs151341331
Gnomadrs151341331
Varsomers151341331
LitVarrs151341331
Maprs151341331
PheGenIrs151341331
Biobankrs151341331
1000 genomesrs151341331
hgdprs151341331
ensemblrs151341331
geneviewrs151341331
scholarrs151341331
googlers151341331
pharmgkbrs151341331
gwascentralrs151341331
openSNPrs151341331
23andMers151341331
SNPshotrs151341331
SNPdbers151341331
MSV3drs151341331
GWAS Ctlgrs151341331
Max Magnitude0
ClinVar
Risk rs151341331(A;A)
Alt rs151341331(A;A)
Reference Rs151341331(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323963C>T
CLNSRC
CLNACC