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rs151341341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs151341341(-;C)
Make rs151341341(C;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323362
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341341
dbSNP (classic)rs151341341
ClinGenrs151341341
ebirs151341341
HLIrs151341341
Exacrs151341341
Gnomadrs151341341
Varsomers151341341
LitVarrs151341341
Maprs151341341
PheGenIrs151341341
Biobankrs151341341
1000 genomesrs151341341
hgdprs151341341
ensemblrs151341341
geneviewrs151341341
scholarrs151341341
googlers151341341
pharmgkbrs151341341
gwascentralrs151341341
openSNPrs151341341
23andMers151341341
SNPshotrs151341341
SNPdbers151341341
MSV3drs151341341
GWAS Ctlgrs151341341
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341341(C;C)
Alt rs151341341(C;C)
Reference Rs151341341(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323362_31323363insG
CLNSRC
CLNACC