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rs151341300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341300(A;A)
Make rs151341300(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356257
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341300
dbSNP (classic)rs151341300
ClinGenrs151341300
ebirs151341300
HLIrs151341300
Exacrs151341300
Gnomadrs151341300
Varsomers151341300
LitVarrs151341300
Maprs151341300
PheGenIrs151341300
Biobankrs151341300
1000 genomesrs151341300
hgdprs151341300
ensemblrs151341300
geneviewrs151341300
scholarrs151341300
googlers151341300
pharmgkbrs151341300
gwascentralrs151341300
openSNPrs151341300
23andMers151341300
SNPshotrs151341300
SNPdbers151341300
MSV3drs151341300
GWAS Ctlgrs151341300
Max Magnitude0
ClinVar
Risk rs151341300(A;A)
Alt rs151341300(A;A)
Reference Rs151341300(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324034C>T
CLNSRC
CLNACC