rs730881063
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs730881063(A;T) |
| Make rs730881063(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 3 |
| Position | 52454008 |
| Gene | NISCH, TNNC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs730881063 |
| dbSNP (classic) | rs730881063 |
| ClinGen | rs730881063 |
| ebi | rs730881063 |
| HLI | rs730881063 |
| Exac | rs730881063 |
| Gnomad | rs730881063 |
| Varsome | rs730881063 |
| LitVar | rs730881063 |
| Map | rs730881063 |
| PheGenI | rs730881063 |
| Biobank | rs730881063 |
| 1000 genomes | rs730881063 |
| hgdp | rs730881063 |
| ensembl | rs730881063 |
| geneview | rs730881063 |
| scholar | rs730881063 |
| rs730881063 | |
| pharmgkb | rs730881063 |
| gwascentral | rs730881063 |
| openSNP | rs730881063 |
| 23andMe | rs730881063 |
| SNPshot | rs730881063 |
| SNPdbe | rs730881063 |
| MSV3d | rs730881063 |
| GWAS Ctlg | rs730881063 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs730881063(T;T) |
| Alt | rs730881063(T;T) |
| Reference | Rs730881063(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TNNC1 NISCH |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000003.11:g.52488024T>A |
| CLNSRC | |
| CLNACC | RCV000159203.2, |
