rs4309
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs4309(C;T) |
Make rs4309(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 63482562 |
Gene | ACE |
is a | snp |
is | mentioned by |
dbSNP | rs4309 |
dbSNP (classic) | rs4309 |
ClinGen | rs4309 |
ebi | rs4309 |
HLI | rs4309 |
Exac | rs4309 |
Gnomad | rs4309 |
Varsome | rs4309 |
LitVar | rs4309 |
Map | rs4309 |
PheGenI | rs4309 |
Biobank | rs4309 |
1000 genomes | rs4309 |
hgdp | rs4309 |
ensembl | rs4309 |
geneview | rs4309 |
scholar | rs4309 |
rs4309 | |
pharmgkb | rs4309 |
gwascentral | rs4309 |
openSNP | rs4309 |
23andMe | rs4309 |
SNPshot | rs4309 |
SNPdbe | rs4309 |
MSV3d | rs4309 |
GWAS Ctlg | rs4309 |
GMAF | 0.421 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20854388] Investigation of ACE, ACE2 and AGTR1 genes for association with nephropathy in Typeâ??1 diabetes mellitus
[PMID 17092869] Haplotype structure of five SNPs within the ACE gene in the Tunisian population.
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
[PMID 19132786] Angiotensin-converting enzyme gene does not contribute to genetic susceptibility to systemic sclerosis in European Caucasians.
[PMID 20215856] Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head.
[PMID 26403748] [Association between angiotensin-converting enzyme gene polymorphism and Alzheimer's disease]
[PMID 26436397] Correlation between single nucleotide polymorphisms in hypoxia-related genes and susceptibility to acute high-altitude pulmonary edema
ClinVar | |
---|---|
Risk | rs4309(T;T) |
Alt | rs4309(T;T) |
Reference | Rs4309(C;C) |
Significance | Non-pathogenic |
Disease | not specified Renal dysplasia |
Variation | info |
Gene | ACE |
CLNDBN | not specified Renal dysplasia |
Reversed | 0 |
HGVS | NC_000017.10:g.61559923C>T |
CLNSRC | |
CLNACC | RCV000247405.1, RCV000287918.1, |
[PMID 30254660] MS4A2-rs573790 Is Associated With Aspirin-Exacerbated Respiratory Disease: Replicative Study Using a Candidate Gene Strategy.