rs7968682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7968682(G;G) |
| Make rs7968682(G;T) |
| Make rs7968682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 65978100 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7968682 |
| dbSNP (classic) | rs7968682 |
| ClinGen | rs7968682 |
| ebi | rs7968682 |
| HLI | rs7968682 |
| Exac | rs7968682 |
| Gnomad | rs7968682 |
| Varsome | rs7968682 |
| LitVar | rs7968682 |
| Map | rs7968682 |
| PheGenI | rs7968682 |
| Biobank | rs7968682 |
| 1000 genomes | rs7968682 |
| hgdp | rs7968682 |
| ensembl | rs7968682 |
| geneview | rs7968682 |
| scholar | rs7968682 |
| rs7968682 | |
| pharmgkb | rs7968682 |
| gwascentral | rs7968682 |
| openSNP | rs7968682 |
| 23andMe | rs7968682 |
| SNPshot | rs7968682 |
| SNPdbe | rs7968682 |
| MSV3d | rs7968682 |
| GWAS Ctlg | rs7968682 |
| GMAF | 0.3329 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22021425 ]
|
| Trait | |
| Title | Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe). |
| Risk Allele | T |
| P-val | 4E-10 |
| Odds Ratio | 0.0430 None |
[PMID 18193045] Common variants in the GDF5-UQCC region are associated with variation in human height.
[PMID 19132395] Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.
[PMID 19930247] HMGA2 is confirmed to be associated with human adult height.
