rs7605378
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7605378(A;A) |
| Make rs7605378(A;C) |
| Make rs7605378(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 199812203 |
| Gene | FTCDNL1, LOC105373832 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7605378 |
| dbSNP (classic) | rs7605378 |
| ClinGen | rs7605378 |
| ebi | rs7605378 |
| HLI | rs7605378 |
| Exac | rs7605378 |
| Gnomad | rs7605378 |
| Varsome | rs7605378 |
| LitVar | rs7605378 |
| Map | rs7605378 |
| PheGenI | rs7605378 |
| Biobank | rs7605378 |
| 1000 genomes | rs7605378 |
| hgdp | rs7605378 |
| ensembl | rs7605378 |
| geneview | rs7605378 |
| scholar | rs7605378 |
| rs7605378 | |
| pharmgkb | rs7605378 |
| gwascentral | rs7605378 |
| openSNP | rs7605378 |
| 23andMe | rs7605378 |
| SNPshot | rs7605378 |
| SNPdbe | rs7605378 |
| MSV3d | rs7605378 |
| GWAS Ctlg | rs7605378 |
| GMAF | 0.388 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21573128
] Common Variants in a Novel Gene, FONG on Chromosome 2q33.1 Confer Risk of Osteoporosis in Japanese
