rs190494527
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs190494527(A;A) |
Make rs190494527(A;G) |
Make rs190494527(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 93556396 |
Gene | GPC6 |
is a | snp |
is | mentioned by |
dbSNP | rs190494527 |
dbSNP (classic) | rs190494527 |
ClinGen | rs190494527 |
ebi | rs190494527 |
HLI | rs190494527 |
Exac | rs190494527 |
Gnomad | rs190494527 |
Varsome | rs190494527 |
LitVar | rs190494527 |
Map | rs190494527 |
PheGenI | rs190494527 |
Biobank | rs190494527 |
1000 genomes | rs190494527 |
hgdp | rs190494527 |
ensembl | rs190494527 |
geneview | rs190494527 |
scholar | rs190494527 |
rs190494527 | |
pharmgkb | rs190494527 |
gwascentral | rs190494527 |
openSNP | rs190494527 |
23andMe | rs190494527 |
SNPshot | rs190494527 |
SNPdbe | rs190494527 |
MSV3d | rs190494527 |
GWAS Ctlg | rs190494527 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (asymmetric/symetric ratio) |
Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Risk Allele | G |
P-val | 7E-6 |
Odds Ratio | .18 [0.099-0.251] unit increase |