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rs490556

From SNPedia

Orientationminus
Stabilizedminus
Make rs490556(C;C)
Make rs490556(C;T)
Make rs490556(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position4022536
is asnp
is mentioned by
dbSNPrs490556
ebirs490556
HLIrs490556
Exacrs490556
Varsomers490556
Maprs490556
PheGenIrs490556
hapmaprs490556
1000 genomesrs490556
hgdprs490556
ensemblrs490556
gopubmedrs490556
geneviewrs490556
scholarrs490556
googlers490556
pharmgkbrs490556
gwascentralrs490556
openSNPrs490556
23andMers490556
23andMe allrs490556
SNP Nexus

SNPshotrs490556
SNPdbers490556
MSV3drs490556
GWAS Ctlgrs490556
GMAF0.3889
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21107343] SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population