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rs45627342

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45627342(-;-)
Make rs45627342(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324370
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45627342
ebirs45627342
HLIrs45627342
Exacrs45627342
Varsomers45627342
Maprs45627342
PheGenIrs45627342
hapmaprs45627342
1000 genomesrs45627342
hgdprs45627342
ensemblrs45627342
gopubmedrs45627342
geneviewrs45627342
scholarrs45627342
googlers45627342
pharmgkbrs45627342
gwascentralrs45627342
openSNPrs45627342
23andMers45627342
23andMe allrs45627342
SNP Nexus

SNPshotrs45627342
SNPdbers45627342
MSV3drs45627342
GWAS Ctlgrs45627342
StatusDeleted
Max Magnitude0
ClinVar
Risk rs45627342(;)
Alt rs45627342(;)
Reference rs45627342(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324370delG
CLNSRC
CLNACC