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rs151341236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341236(C;T)
Make rs151341236(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356381
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341236
dbSNP (classic)rs151341236
ClinGenrs151341236
ebirs151341236
HLIrs151341236
Exacrs151341236
Gnomadrs151341236
Varsomers151341236
LitVarrs151341236
Maprs151341236
PheGenIrs151341236
Biobankrs151341236
1000 genomesrs151341236
hgdprs151341236
ensemblrs151341236
geneviewrs151341236
scholarrs151341236
googlers151341236
pharmgkbrs151341236
gwascentralrs151341236
openSNPrs151341236
23andMers151341236
SNPshotrs151341236
SNPdbers151341236
MSV3drs151341236
GWAS Ctlgrs151341236
Max Magnitude0
ClinVar
Risk rs151341236(T;T)
Alt rs151341236(T;T)
Reference Rs151341236(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324158G>A
CLNSRC
CLNACC