rs17047573
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs17047573(G;G) |
| Make rs17047573(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 68361969 |
| Gene | FAM19A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17047573 |
| dbSNP (classic) | rs17047573 |
| ClinGen | rs17047573 |
| ebi | rs17047573 |
| HLI | rs17047573 |
| Exac | rs17047573 |
| Gnomad | rs17047573 |
| Varsome | rs17047573 |
| LitVar | rs17047573 |
| Map | rs17047573 |
| PheGenI | rs17047573 |
| Biobank | rs17047573 |
| 1000 genomes | rs17047573 |
| hgdp | rs17047573 |
| ensembl | rs17047573 |
| geneview | rs17047573 |
| scholar | rs17047573 |
| rs17047573 | |
| pharmgkb | rs17047573 |
| gwascentral | rs17047573 |
| openSNP | rs17047573 |
| 23andMe | rs17047573 |
| SNPshot | rs17047573 |
| SNPdbe | rs17047573 |
| MSV3d | rs17047573 |
| GWAS Ctlg | rs17047573 |
| GMAF | 0.0854 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20664687
] Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract
