rs34621387
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs34621387(A;A) |
| Make rs34621387(A;G) |
| Make rs34621387(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 12 |
| Position | 2419238 |
| Gene | CACNA1C |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34621387 |
| dbSNP (classic) | rs34621387 |
| ClinGen | rs34621387 |
| ebi | rs34621387 |
| HLI | rs34621387 |
| Exac | rs34621387 |
| Gnomad | rs34621387 |
| Varsome | rs34621387 |
| LitVar | rs34621387 |
| Map | rs34621387 |
| PheGenI | rs34621387 |
| Biobank | rs34621387 |
| 1000 genomes | rs34621387 |
| hgdp | rs34621387 |
| ensembl | rs34621387 |
| geneview | rs34621387 |
| scholar | rs34621387 |
| rs34621387 | |
| pharmgkb | rs34621387 |
| gwascentral | rs34621387 |
| openSNP | rs34621387 |
| 23andMe | rs34621387 |
| SNPshot | rs34621387 |
| SNPdbe | rs34621387 |
| MSV3d | rs34621387 |
| GWAS Ctlg | rs34621387 |
| Max Magnitude | 0 |
[PMID 27123490
] DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient.
