rs1046276
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1046276(C;C) |
| Make rs1046276(C;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 30903305 |
| Gene | CTF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1046276 |
| dbSNP (classic) | rs1046276 |
| ClinGen | rs1046276 |
| ebi | rs1046276 |
| HLI | rs1046276 |
| Exac | rs1046276 |
| Gnomad | rs1046276 |
| Varsome | rs1046276 |
| LitVar | rs1046276 |
| Map | rs1046276 |
| PheGenI | rs1046276 |
| Biobank | rs1046276 |
| 1000 genomes | rs1046276 |
| hgdp | rs1046276 |
| ensembl | rs1046276 |
| geneview | rs1046276 |
| scholar | rs1046276 |
| rs1046276 | |
| pharmgkb | rs1046276 |
| gwascentral | rs1046276 |
| openSNP | rs1046276 |
| 23andMe | rs1046276 |
| SNPshot | rs1046276 |
| SNPdbe | rs1046276 |
| MSV3d | rs1046276 |
| GWAS Ctlg | rs1046276 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25025664
] Common genetic variation in the human CTF1 locus, encoding cardiotrophin-1, determines insulin sensitivity
| ClinVar | |
|---|---|
| Risk | rs1046276(C;C) |
| Alt | rs1046276(C;C) |
| Reference | Rs1046276(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Dilated Cardiomyopathy |
| Variation | info |
| Gene | CTF1 |
| CLNDBN | Dilated Cardiomyopathy, Dominant |
| Reversed | 0 |
| HGVS | NC_000016.9:g.30914626T>C |
| CLNSRC | |
| CLNACC | RCV000359554.1, |
