rs17085159
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17085159(A;A) |
| Make rs17085159(A;G) |
| Make rs17085159(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 95831293 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17085159 |
| dbSNP (classic) | rs17085159 |
| ClinGen | rs17085159 |
| ebi | rs17085159 |
| HLI | rs17085159 |
| Exac | rs17085159 |
| Gnomad | rs17085159 |
| Varsome | rs17085159 |
| LitVar | rs17085159 |
| Map | rs17085159 |
| PheGenI | rs17085159 |
| Biobank | rs17085159 |
| 1000 genomes | rs17085159 |
| hgdp | rs17085159 |
| ensembl | rs17085159 |
| geneview | rs17085159 |
| scholar | rs17085159 |
| rs17085159 | |
| pharmgkb | rs17085159 |
| gwascentral | rs17085159 |
| openSNP | rs17085159 |
| 23andMe | rs17085159 |
| SNPshot | rs17085159 |
| SNPdbe | rs17085159 |
| MSV3d | rs17085159 |
| GWAS Ctlg | rs17085159 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 29399948
] A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.
