rs117576300
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs117576300(A;A) |
Make rs117576300(A;G) |
Make rs117576300(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 82138856 |
Gene | CACNA2D1 |
is a | snp |
is | mentioned by |
dbSNP | rs117576300 |
dbSNP (classic) | rs117576300 |
ClinGen | rs117576300 |
ebi | rs117576300 |
HLI | rs117576300 |
Exac | rs117576300 |
Gnomad | rs117576300 |
Varsome | rs117576300 |
LitVar | rs117576300 |
Map | rs117576300 |
PheGenI | rs117576300 |
Biobank | rs117576300 |
1000 genomes | rs117576300 |
hgdp | rs117576300 |
ensembl | rs117576300 |
geneview | rs117576300 |
scholar | rs117576300 |
rs117576300 | |
pharmgkb | rs117576300 |
gwascentral | rs117576300 |
openSNP | rs117576300 |
23andMe | rs117576300 |
SNPshot | rs117576300 |
SNPdbe | rs117576300 |
MSV3d | rs117576300 |
GWAS Ctlg | rs117576300 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (asymmetric) |
Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Risk Allele | A |
P-val | 6E-6 |
Odds Ratio | .30 [0.17-0.43] unit decrease |