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rs45460800

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45460800(-;-)
Make rs45460800(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324071
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45460800
ebirs45460800
HLIrs45460800
Exacrs45460800
Varsomers45460800
Maprs45460800
PheGenIrs45460800
hapmaprs45460800
1000 genomesrs45460800
hgdprs45460800
ensemblrs45460800
gopubmedrs45460800
geneviewrs45460800
scholarrs45460800
googlers45460800
pharmgkbrs45460800
gwascentralrs45460800
openSNPrs45460800
23andMers45460800
23andMe allrs45460800
SNP Nexus

SNPshotrs45460800
SNPdbers45460800
MSV3drs45460800
GWAS Ctlgrs45460800
StatusDeleted
Max Magnitude0
ClinVar
Risk rs45460800(;)
Alt rs45460800(;)
Reference rs45460800(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324071delA
CLNSRC
CLNACC