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rs45486291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45486291(-;-)
Make rs45486291(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324066
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45486291
ebirs45486291
HLIrs45486291
Exacrs45486291
Varsomers45486291
Maprs45486291
PheGenIrs45486291
hapmaprs45486291
1000 genomesrs45486291
hgdprs45486291
ensemblrs45486291
gopubmedrs45486291
geneviewrs45486291
scholarrs45486291
googlers45486291
pharmgkbrs45486291
gwascentralrs45486291
openSNPrs45486291
23andMers45486291
23andMe allrs45486291
SNP Nexus

SNPshotrs45486291
SNPdbers45486291
MSV3drs45486291
GWAS Ctlgrs45486291
StatusDeleted
Max Magnitude0
ClinVar
Risk rs45486291(;)
Alt rs45486291(;)
Reference rs45486291(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324066delA
CLNSRC
CLNACC