rs3737965
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3737965(C;T) |
Make rs3737965(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 11806394 |
Gene | CLCN6, MTHFR |
is a | snp |
is | mentioned by |
dbSNP | rs3737965 |
dbSNP (classic) | rs3737965 |
ClinGen | rs3737965 |
ebi | rs3737965 |
HLI | rs3737965 |
Exac | rs3737965 |
Gnomad | rs3737965 |
Varsome | rs3737965 |
LitVar | rs3737965 |
Map | rs3737965 |
PheGenI | rs3737965 |
Biobank | rs3737965 |
1000 genomes | rs3737965 |
hgdp | rs3737965 |
ensembl | rs3737965 |
geneview | rs3737965 |
scholar | rs3737965 |
rs3737965 | |
pharmgkb | rs3737965 |
gwascentral | rs3737965 |
openSNP | rs3737965 |
23andMe | rs3737965 |
SNPshot | rs3737965 |
SNPdbe | rs3737965 |
MSV3d | rs3737965 |
GWAS Ctlg | rs3737965 |
GMAF | 0.05188 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26740945] The rs3737964 single-nucleotide polymorphism of the chloride channel-6 gene as a risk factor for coronary heart disease.