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rs151341344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341344(A;A)
Make rs151341344(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355540
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341344
dbSNP (classic)rs151341344
ClinGenrs151341344
ebirs151341344
HLIrs151341344
Exacrs151341344
Gnomadrs151341344
Varsomers151341344
LitVarrs151341344
Maprs151341344
PheGenIrs151341344
Biobankrs151341344
1000 genomesrs151341344
hgdprs151341344
ensemblrs151341344
geneviewrs151341344
scholarrs151341344
googlers151341344
pharmgkbrs151341344
gwascentralrs151341344
openSNPrs151341344
23andMers151341344
SNPshotrs151341344
SNPdbers151341344
MSV3drs151341344
GWAS Ctlgrs151341344
Max Magnitude0
ClinVar
Risk rs151341344(A;A)
Alt rs151341344(A;A)
Reference Rs151341344(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323317G>T
CLNSRC
CLNACC