rs1017
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1017(A;A) |
| Make rs1017(A;T) |
| Make rs1017(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 51394261 |
| Gene | ISL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1017 |
| dbSNP (classic) | rs1017 |
| ClinGen | rs1017 |
| ebi | rs1017 |
| HLI | rs1017 |
| Exac | rs1017 |
| Gnomad | rs1017 |
| Varsome | rs1017 |
| LitVar | rs1017 |
| Map | rs1017 |
| PheGenI | rs1017 |
| Biobank | rs1017 |
| 1000 genomes | rs1017 |
| hgdp | rs1017 |
| ensembl | rs1017 |
| geneview | rs1017 |
| scholar | rs1017 |
| rs1017 | |
| pharmgkb | rs1017 |
| gwascentral | rs1017 |
| openSNP | rs1017 |
| 23andMe | rs1017 |
| SNPshot | rs1017 |
| SNPdbe | rs1017 |
| MSV3d | rs1017 |
| GWAS Ctlg | rs1017 |
| GMAF | 0.3669 |
| Max Magnitude | 0 |
[PMID 22480195
] ISL1 Common Variant rs1017 Is Not Associated with Susceptibility to Congenital Heart Disease in a Chinese Population
[PMID 20520780] Common variation in ISL1 confers genetic susceptibility for human congenital heart disease.
[PMID 23229290] Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.
[PMID 23572340] Association between ISL1 variants and susceptibility to ventricular septal defect in a Chinese cohort.
