rs6632677
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6632677(C;C) |
Make rs6632677(C;G) |
Make rs6632677(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 15596749 |
Gene | ACE2 |
is a | snp |
is | mentioned by |
dbSNP | rs6632677 |
dbSNP (classic) | rs6632677 |
ClinGen | rs6632677 |
ebi | rs6632677 |
HLI | rs6632677 |
Exac | rs6632677 |
Gnomad | rs6632677 |
Varsome | rs6632677 |
LitVar | rs6632677 |
Map | rs6632677 |
PheGenI | rs6632677 |
Biobank | rs6632677 |
1000 genomes | rs6632677 |
hgdp | rs6632677 |
ensembl | rs6632677 |
geneview | rs6632677 |
scholar | rs6632677 |
rs6632677 | |
pharmgkb | rs6632677 |
gwascentral | rs6632677 |
openSNP | rs6632677 |
23andMe | rs6632677 |
SNPshot | rs6632677 |
SNPdbe | rs6632677 |
MSV3d | rs6632677 |
GWAS Ctlg | rs6632677 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 28744816] ACE2, CALM3 and TNNI3K polymorphisms as potential disease modifiers in hypertrophic and dilated cardiomyopathies.
[PMID 29441892] Association of AGTR1 and ACE2 gene polymorphisms with structural atrial fibrillation in a Chinese Han population.