rs45501500
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs45501500(A;A) |
| Make rs45501500(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 201363390 |
| Gene | TNNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs45501500 |
| dbSNP (classic) | rs45501500 |
| ClinGen | rs45501500 |
| ebi | rs45501500 |
| HLI | rs45501500 |
| Exac | rs45501500 |
| Gnomad | rs45501500 |
| Varsome | rs45501500 |
| LitVar | rs45501500 |
| Map | rs45501500 |
| PheGenI | rs45501500 |
| Biobank | rs45501500 |
| 1000 genomes | rs45501500 |
| hgdp | rs45501500 |
| ensembl | rs45501500 |
| geneview | rs45501500 |
| scholar | rs45501500 |
| rs45501500 | |
| pharmgkb | rs45501500 |
| gwascentral | rs45501500 |
| openSNP | rs45501500 |
| 23andMe | rs45501500 |
| SNPshot | rs45501500 |
| SNPdbe | rs45501500 |
| MSV3d | rs45501500 |
| GWAS Ctlg | rs45501500 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs45501500(A;A) |
| Alt | rs45501500(A;A) |
| Reference | Rs45501500(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | TNNT2 |
| CLNDBN | not specified not provided |
| Reversed | 1 |
| HGVS | NC_000001.10:g.201332518C>T |
| CLNSRC | |
| CLNACC | RCV000036595.3, RCV000225721.1, |
