rs374528680
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs374528680(C;C) |
| Make rs374528680(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 2686216 |
| Gene | CACNA1C, CACNA1C-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs374528680 |
| dbSNP (classic) | rs374528680 |
| ClinGen | rs374528680 |
| ebi | rs374528680 |
| HLI | rs374528680 |
| Exac | rs374528680 |
| Gnomad | rs374528680 |
| Varsome | rs374528680 |
| LitVar | rs374528680 |
| Map | rs374528680 |
| PheGenI | rs374528680 |
| Biobank | rs374528680 |
| 1000 genomes | rs374528680 |
| hgdp | rs374528680 |
| ensembl | rs374528680 |
| geneview | rs374528680 |
| scholar | rs374528680 |
| rs374528680 | |
| pharmgkb | rs374528680 |
| gwascentral | rs374528680 |
| openSNP | rs374528680 |
| 23andMe | rs374528680 |
| SNPshot | rs374528680 |
| SNPdbe | rs374528680 |
| MSV3d | rs374528680 |
| GWAS Ctlg | rs374528680 |
| Max Magnitude | 0 |
[PMID 25184293
] A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis
| ClinVar | |
|---|---|
| Risk | rs374528680(C;C) |
| Alt | rs374528680(C;C) |
| Reference | Rs374528680(G;G) |
| Significance | Unknown |
| Disease | not provided Long QT syndrome not specified |
| Variation | info |
| Gene | CACNA1C-AS1 CACNA1C |
| CLNDBN | not provided Long QT syndrome not specified |
| Reversed | 0 |
| HGVS | NC_000012.11:g.2795382G>C |
| CLNSRC | |
| CLNACC | RCV000171619.3, RCV000226828.1, RCV000259175.1, |
