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rs41562416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562416(-;-)
Make rs41562416(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324591
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562416
ebirs41562416
HLIrs41562416
Exacrs41562416
Varsomers41562416
Maprs41562416
PheGenIrs41562416
hapmaprs41562416
1000 genomesrs41562416
hgdprs41562416
ensemblrs41562416
gopubmedrs41562416
geneviewrs41562416
scholarrs41562416
googlers41562416
pharmgkbrs41562416
gwascentralrs41562416
openSNPrs41562416
23andMers41562416
23andMe allrs41562416
SNP Nexus

SNPshotrs41562416
SNPdbers41562416
MSV3drs41562416
GWAS Ctlgrs41562416
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41562416(;)
Alt rs41562416(;)
Reference rs41562416(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324591delC
CLNSRC
CLNACC