rs1708299
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1708299(C;C) |
| Make rs1708299(C;T) |
| Make rs1708299(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 28150327 |
| Gene | JAZF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1708299 |
| dbSNP (classic) | rs1708299 |
| ClinGen | rs1708299 |
| ebi | rs1708299 |
| HLI | rs1708299 |
| Exac | rs1708299 |
| Gnomad | rs1708299 |
| Varsome | rs1708299 |
| LitVar | rs1708299 |
| Map | rs1708299 |
| PheGenI | rs1708299 |
| Biobank | rs1708299 |
| 1000 genomes | rs1708299 |
| hgdp | rs1708299 |
| ensembl | rs1708299 |
| geneview | rs1708299 |
| scholar | rs1708299 |
| rs1708299 | |
| pharmgkb | rs1708299 |
| gwascentral | rs1708299 |
| openSNP | rs1708299 |
| 23andMe | rs1708299 |
| SNPshot | rs1708299 |
| SNPdbe | rs1708299 |
| MSV3d | rs1708299 |
| GWAS Ctlg | rs1708299 |
| GMAF | 0.146 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 6E-25 |
| Odds Ratio | .04 [NR] unit increase |
