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rs45626438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45626438(A;A)
Make rs45626438(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271284
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45626438
ebirs45626438
HLIrs45626438
Exacrs45626438
Varsomers45626438
Maprs45626438
PheGenIrs45626438
hapmaprs45626438
1000 genomesrs45626438
hgdprs45626438
ensemblrs45626438
gopubmedrs45626438
geneviewrs45626438
scholarrs45626438
googlers45626438
pharmgkbrs45626438
gwascentralrs45626438
openSNPrs45626438
23andMers45626438
23andMe allrs45626438
SNP Nexus

SNPshotrs45626438
SNPdbers45626438
MSV3drs45626438
GWAS Ctlgrs45626438
Max Magnitude0
ClinVar
Risk rs45626438(A,C,T;A,C,T)
Alt rs45626438(A,C,T;A,C,T)
Reference rs45626438(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239061C>A; NC_000006.11:g.31239061C>G; NC_000006.11:g.31239061C>T
CLNSRC
CLNACC