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rs151341195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341195(C;T)
Make rs151341195(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356741
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341195
dbSNP (classic)rs151341195
ClinGenrs151341195
ebirs151341195
HLIrs151341195
Exacrs151341195
Gnomadrs151341195
Varsomers151341195
LitVarrs151341195
Maprs151341195
PheGenIrs151341195
Biobankrs151341195
1000 genomesrs151341195
hgdprs151341195
ensemblrs151341195
geneviewrs151341195
scholarrs151341195
googlers151341195
pharmgkbrs151341195
gwascentralrs151341195
openSNPrs151341195
23andMers151341195
SNPshotrs151341195
SNPdbers151341195
MSV3drs151341195
GWAS Ctlgrs151341195
Max Magnitude0
ClinVar
Risk rs151341195(T;T)
Alt rs151341195(T;T)
Reference Rs151341195(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324518G>A
CLNSRC
CLNACC