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rs151341335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341335(C;G)
Make rs151341335(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356171
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341335
dbSNP (classic)rs151341335
ClinGenrs151341335
ebirs151341335
HLIrs151341335
Exacrs151341335
Gnomadrs151341335
Varsomers151341335
LitVarrs151341335
Maprs151341335
PheGenIrs151341335
Biobankrs151341335
1000 genomesrs151341335
hgdprs151341335
ensemblrs151341335
geneviewrs151341335
scholarrs151341335
googlers151341335
pharmgkbrs151341335
gwascentralrs151341335
openSNPrs151341335
23andMers151341335
SNPshotrs151341335
SNPdbers151341335
MSV3drs151341335
GWAS Ctlgrs151341335
Max Magnitude0
ClinVar
Risk rs151341335(G;G)
Alt rs151341335(G;G)
Reference Rs151341335(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323948G>C
CLNSRC
CLNACC