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rs45609431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45609431(A;A)
Make rs45609431(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271664
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45609431
ebirs45609431
HLIrs45609431
Exacrs45609431
Varsomers45609431
Maprs45609431
PheGenIrs45609431
hapmaprs45609431
1000 genomesrs45609431
hgdprs45609431
ensemblrs45609431
gopubmedrs45609431
geneviewrs45609431
scholarrs45609431
googlers45609431
pharmgkbrs45609431
gwascentralrs45609431
openSNPrs45609431
23andMers45609431
23andMe allrs45609431
SNP Nexus

SNPshotrs45609431
SNPdbers45609431
MSV3drs45609431
GWAS Ctlgrs45609431
Max Magnitude0
ClinVar
Risk rs45609431(A;A)
Alt rs45609431(A;A)
Reference rs45609431(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239441C>T
CLNSRC
CLNACC