rs757608
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs757608(C;C) |
| Make rs757608(C;T) |
| Make rs757608(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 61419916 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757608 |
| dbSNP (classic) | rs757608 |
| ClinGen | rs757608 |
| ebi | rs757608 |
| HLI | rs757608 |
| Exac | rs757608 |
| Gnomad | rs757608 |
| Varsome | rs757608 |
| LitVar | rs757608 |
| Map | rs757608 |
| PheGenI | rs757608 |
| Biobank | rs757608 |
| 1000 genomes | rs757608 |
| hgdp | rs757608 |
| ensembl | rs757608 |
| geneview | rs757608 |
| scholar | rs757608 |
| rs757608 | |
| pharmgkb | rs757608 |
| gwascentral | rs757608 |
| openSNP | rs757608 |
| 23andMe | rs757608 |
| SNPshot | rs757608 |
| SNPdbe | rs757608 |
| MSV3d | rs757608 |
| GWAS Ctlg | rs757608 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | T |
| P-val | 5.9999999999999995E-8 |
| Odds Ratio | 4.40 [2.83-5.97] % SD taller |
[PMID 19030899
] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
[PMID 19039035] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
[PMID 20027299] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
