rs4404477
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4404477(A;A) |
Make rs4404477(A;G) |
Make rs4404477(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 117655921 |
Gene | LSAMP |
is a | snp |
is | mentioned by |
dbSNP | rs4404477 |
dbSNP (classic) | rs4404477 |
ClinGen | rs4404477 |
ebi | rs4404477 |
HLI | rs4404477 |
Exac | rs4404477 |
Gnomad | rs4404477 |
Varsome | rs4404477 |
LitVar | rs4404477 |
Map | rs4404477 |
PheGenI | rs4404477 |
Biobank | rs4404477 |
1000 genomes | rs4404477 |
hgdp | rs4404477 |
ensembl | rs4404477 |
geneview | rs4404477 |
scholar | rs4404477 |
rs4404477 | |
pharmgkb | rs4404477 |
gwascentral | rs4404477 |
openSNP | rs4404477 |
23andMe | rs4404477 |
SNPshot | rs4404477 |
SNPdbe | rs4404477 |
MSV3d | rs4404477 |
GWAS Ctlg | rs4404477 |
GMAF | 0.27 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18318786],AEHA 2008 ppt - rs4404477(A)/rs1676232(A) defines a significant left main coronary artery disease risk haplotype