rs876661393
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs876661393(A;A) |
| Make rs876661393(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 52452147 |
| Gene | TNNC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs876661393 |
| dbSNP (classic) | rs876661393 |
| ClinGen | rs876661393 |
| ebi | rs876661393 |
| HLI | rs876661393 |
| Exac | rs876661393 |
| Gnomad | rs876661393 |
| Varsome | rs876661393 |
| LitVar | rs876661393 |
| Map | rs876661393 |
| PheGenI | rs876661393 |
| Biobank | rs876661393 |
| 1000 genomes | rs876661393 |
| hgdp | rs876661393 |
| ensembl | rs876661393 |
| geneview | rs876661393 |
| scholar | rs876661393 |
| rs876661393 | |
| pharmgkb | rs876661393 |
| gwascentral | rs876661393 |
| openSNP | rs876661393 |
| 23andMe | rs876661393 |
| SNPshot | rs876661393 |
| SNPdbe | rs876661393 |
| MSV3d | rs876661393 |
| GWAS Ctlg | rs876661393 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs876661393(A;A) |
| Alt | rs876661393(A;A) |
| Reference | Rs876661393(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | TNNC1 |
| CLNDBN | not specified not provided |
| Reversed | 1 |
| HGVS | NC_000003.11:g.52486163G>T |
| CLNSRC | |
| CLNACC | RCV000223755.1, RCV000483835.1, |
