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rs151341383

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341383(-;-)
Make rs151341383(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323099
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341383
dbSNP (classic)rs151341383
ClinGenrs151341383
ebirs151341383
HLIrs151341383
Exacrs151341383
Gnomadrs151341383
Varsomers151341383
LitVarrs151341383
Maprs151341383
PheGenIrs151341383
Biobankrs151341383
1000 genomesrs151341383
hgdprs151341383
ensemblrs151341383
geneviewrs151341383
scholarrs151341383
googlers151341383
pharmgkbrs151341383
gwascentralrs151341383
openSNPrs151341383
23andMers151341383
SNPshotrs151341383
SNPdbers151341383
MSV3drs151341383
GWAS Ctlgrs151341383
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341383(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323099delC
CLNSRC
CLNACC