rs368200299
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs368200299(A;A) |
| Make rs368200299(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 2 |
| Position | 178620285 |
| Gene | TTN, TTN-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs368200299 |
| dbSNP (classic) | rs368200299 |
| ClinGen | rs368200299 |
| ebi | rs368200299 |
| HLI | rs368200299 |
| Exac | rs368200299 |
| Gnomad | rs368200299 |
| Varsome | rs368200299 |
| LitVar | rs368200299 |
| Map | rs368200299 |
| PheGenI | rs368200299 |
| Biobank | rs368200299 |
| 1000 genomes | rs368200299 |
| hgdp | rs368200299 |
| ensembl | rs368200299 |
| geneview | rs368200299 |
| scholar | rs368200299 |
| rs368200299 | |
| pharmgkb | rs368200299 |
| gwascentral | rs368200299 |
| openSNP | rs368200299 |
| 23andMe | rs368200299 |
| SNPshot | rs368200299 |
| SNPdbe | rs368200299 |
| MSV3d | rs368200299 |
| GWAS Ctlg | rs368200299 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs368200299(A;A) rs368200299(T;T) |
| Alt | rs368200299(A;A) rs368200299(T;T) |
| Reference | Rs368200299(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Dilated cardiomyopathy 1G Familial hypertrophic cardiomyopathy 9 Primary dilated cardiomyopathy |
| Variation | info |
| Gene | TTN TTN-AS1 |
| CLNDBN | Dilated cardiomyopathy 1G Familial hypertrophic cardiomyopathy 9 Primary dilated cardiomyopathy |
| Reversed | 0 |
| HGVS | NC_000002.11:g.179485012G>T |
| CLNSRC | |
| CLNACC | RCV000196059.1, RCV000209311.1, |
