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rs5875314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs5875314(-;-)
Make rs5875314(-;C)
Make rs5875314(C;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324247
GeneHLA-B
is asnp
is mentioned by
dbSNPrs5875314
ebirs5875314
HLIrs5875314
Exacrs5875314
Varsomers5875314
Maprs5875314
PheGenIrs5875314
hapmaprs5875314
1000 genomesrs5875314
hgdprs5875314
ensemblrs5875314
gopubmedrs5875314
geneviewrs5875314
scholarrs5875314
googlers5875314
pharmgkbrs5875314
gwascentralrs5875314
openSNPrs5875314
23andMers5875314
23andMe allrs5875314
SNP Nexus

SNPshotrs5875314
SNPdbers5875314
MSV3drs5875314
GWAS Ctlgrs5875314
Max Magnitude0
ClinVar
Risk rs5875314(C;C)
Alt rs5875314(C;C)
Reference rs5875314(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324247_31324248insC
CLNSRC
CLNACC