rs976683
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs976683(A;A) |
| Make rs976683(A;G) |
| Make rs976683(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 173767581 |
| Gene | NLGN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs976683 |
| dbSNP (classic) | rs976683 |
| ClinGen | rs976683 |
| ebi | rs976683 |
| HLI | rs976683 |
| Exac | rs976683 |
| Gnomad | rs976683 |
| Varsome | rs976683 |
| LitVar | rs976683 |
| Map | rs976683 |
| PheGenI | rs976683 |
| Biobank | rs976683 |
| 1000 genomes | rs976683 |
| hgdp | rs976683 |
| ensembl | rs976683 |
| geneview | rs976683 |
| scholar | rs976683 |
| rs976683 | |
| pharmgkb | rs976683 |
| gwascentral | rs976683 |
| openSNP | rs976683 |
| 23andMe | rs976683 |
| SNPshot | rs976683 |
| SNPdbe | rs976683 |
| MSV3d | rs976683 |
| GWAS Ctlg | rs976683 |
| GMAF | 0.4601 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23929743
] Genome-Wide Analysis of Blood Pressure Variability and Ischemic Stroke
[PMID 20070850] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
