Have questions? Visit https://www.reddit.com/r/SNPedia

rs45496696

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45496696(-;-)
Make rs45496696(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356958
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45496696
ebirs45496696
HLIrs45496696
Exacrs45496696
Varsomers45496696
Maprs45496696
PheGenIrs45496696
hapmaprs45496696
1000 genomesrs45496696
hgdprs45496696
ensemblrs45496696
gopubmedrs45496696
geneviewrs45496696
scholarrs45496696
googlers45496696
pharmgkbrs45496696
gwascentralrs45496696
openSNPrs45496696
23andMers45496696
23andMe allrs45496696
SNP Nexus

SNPshotrs45496696
SNPdbers45496696
MSV3drs45496696
GWAS Ctlgrs45496696
Max Magnitude0
ClinVar
Risk rs45496696(;)
Alt rs45496696(;)
Reference rs45496696(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324735delC
CLNSRC
CLNACC