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rs4461142

From SNPedia

Orientationplus
Stabilizedplus
Make rs4461142(C;C)
Make rs4461142(C;T)
Make rs4461142(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position63500687
is asnp
is mentioned by
dbSNPrs4461142
dbSNP (classic)rs4461142
ClinGenrs4461142
ebirs4461142
HLIrs4461142
Exacrs4461142
Gnomadrs4461142
Varsomers4461142
LitVarrs4461142
Maprs4461142
PheGenIrs4461142
Biobankrs4461142
1000 genomesrs4461142
hgdprs4461142
ensemblrs4461142
geneviewrs4461142
scholarrs4461142
googlers4461142
pharmgkbrs4461142
gwascentralrs4461142
openSNPrs4461142
23andMers4461142
SNPshotrs4461142
SNPdbers4461142
MSV3drs4461142
GWAS Ctlgrs4461142
GMAF0.3572
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23603420] Polymorphisms of Angiotensin converting enzyme and nitric oxide synthase 3 genes as risk factors of high-altitude pulmonary edema: a case-control study and meta-analysis


[PMID 20215856OA-icon.png] Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head.


[PMID 21258267] Angiotensin-converting enzyme tag single nucleotide polymorphisms in patients with intracerebral hemorrhage.