rs8007661
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8007661(C;C) |
| Make rs8007661(C;T) |
| Make rs8007661(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 91993614 |
| Gene | TRIP11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8007661 |
| dbSNP (classic) | rs8007661 |
| ClinGen | rs8007661 |
| ebi | rs8007661 |
| HLI | rs8007661 |
| Exac | rs8007661 |
| Gnomad | rs8007661 |
| Varsome | rs8007661 |
| LitVar | rs8007661 |
| Map | rs8007661 |
| PheGenI | rs8007661 |
| Biobank | rs8007661 |
| 1000 genomes | rs8007661 |
| hgdp | rs8007661 |
| ensembl | rs8007661 |
| geneview | rs8007661 |
| scholar | rs8007661 |
| rs8007661 | |
| pharmgkb | rs8007661 |
| gwascentral | rs8007661 |
| openSNP | rs8007661 |
| 23andMe | rs8007661 |
| SNPshot | rs8007661 |
| SNPdbe | rs8007661 |
| MSV3d | rs8007661 |
| GWAS Ctlg | rs8007661 |
| GMAF | 0.4821 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs8007661 |
| PubMedID | [PMID 18391950 ]
|
| Condition | Height |
| Gene | TRIP11,ATXN3 |
| Risk Allele | T |
| pValue | 6.00E-010 |
| OR | 0.42 |
| 95% CI | 0.30-0.54) cm shorte |
[PMID 19039035] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
