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
] 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, | 


