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rs151341293

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341293(-;-)
Make rs151341293(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356259
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341293
dbSNP (classic)rs151341293
ClinGenrs151341293
ebirs151341293
HLIrs151341293
Exacrs151341293
Gnomadrs151341293
Varsomers151341293
LitVarrs151341293
Maprs151341293
PheGenIrs151341293
Biobankrs151341293
1000 genomesrs151341293
hgdprs151341293
ensemblrs151341293
geneviewrs151341293
scholarrs151341293
googlers151341293
pharmgkbrs151341293
gwascentralrs151341293
openSNPrs151341293
23andMers151341293
SNPshotrs151341293
SNPdbers151341293
MSV3drs151341293
GWAS Ctlgrs151341293
Merged fromRs151341294
GMAF0.4091
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341293(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324036delT
CLNSRC
CLNACC