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rs45500292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs45500292(A;C)
Make rs45500292(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271655
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45500292
ebirs45500292
HLIrs45500292
Exacrs45500292
Varsomers45500292
Maprs45500292
PheGenIrs45500292
hapmaprs45500292
1000 genomesrs45500292
hgdprs45500292
ensemblrs45500292
gopubmedrs45500292
geneviewrs45500292
scholarrs45500292
googlers45500292
pharmgkbrs45500292
gwascentralrs45500292
openSNPrs45500292
23andMers45500292
23andMe allrs45500292
SNP Nexus

SNPshotrs45500292
SNPdbers45500292
MSV3drs45500292
GWAS Ctlgrs45500292
Max Magnitude0
ClinVar
Risk rs45500292(C;C)
Alt rs45500292(C;C)
Reference rs45500292(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239432T>G
CLNSRC
CLNACC