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

rs45504795

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45504795(-;-)
Make rs45504795(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324371
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45504795
ebirs45504795
HLIrs45504795
Exacrs45504795
Varsomers45504795
Maprs45504795
PheGenIrs45504795
hapmaprs45504795
1000 genomesrs45504795
hgdprs45504795
ensemblrs45504795
gopubmedrs45504795
geneviewrs45504795
scholarrs45504795
googlers45504795
pharmgkbrs45504795
gwascentralrs45504795
openSNPrs45504795
23andMers45504795
23andMe allrs45504795
SNP Nexus

SNPshotrs45504795
SNPdbers45504795
MSV3drs45504795
GWAS Ctlgrs45504795
StatusDeleted
Max Magnitude0
ClinVar
Risk rs45504795(;)
Alt rs45504795(;)
Reference rs45504795(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324371delG
CLNSRC
CLNACC