rs200098356
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs200098356(A;A) |
| Make rs200098356(A;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 1860203 |
| Gene | CACNA2D4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs200098356 |
| dbSNP (classic) | rs200098356 |
| ClinGen | rs200098356 |
| ebi | rs200098356 |
| HLI | rs200098356 |
| Exac | rs200098356 |
| Gnomad | rs200098356 |
| Varsome | rs200098356 |
| LitVar | rs200098356 |
| Map | rs200098356 |
| PheGenI | rs200098356 |
| Biobank | rs200098356 |
| 1000 genomes | rs200098356 |
| hgdp | rs200098356 |
| ensembl | rs200098356 |
| geneview | rs200098356 |
| scholar | rs200098356 |
| rs200098356 | |
| pharmgkb | rs200098356 |
| gwascentral | rs200098356 |
| openSNP | rs200098356 |
| 23andMe | rs200098356 |
| SNPshot | rs200098356 |
| SNPdbe | rs200098356 |
| MSV3d | rs200098356 |
| GWAS Ctlg | rs200098356 |
| Max Magnitude | 0 |
OMIM pathogenic variant
