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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
ebirs151341383
HLIrs151341383
Exacrs151341383
Varsomers151341383
Maprs151341383
PheGenIrs151341383
hapmaprs151341383
1000 genomesrs151341383
hgdprs151341383
ensemblrs151341383
gopubmedrs151341383
geneviewrs151341383
scholarrs151341383
googlers151341383
pharmgkbrs151341383
gwascentralrs151341383
openSNPrs151341383
23andMers151341383
23andMe allrs151341383
SNP Nexus

SNPshotrs151341383
SNPdbers151341383
MSV3drs151341383
GWAS Ctlgrs151341383
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341383(;)
Alt rs151341383(;)
Reference rs151341383(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323099delC
CLNSRC
CLNACC