| GWAS snp
|
| PMID
|
[PMID 18391951]
|
| Trait
|
Height
|
| Title
|
Many sequence variants affecting diversity of adult human height
|
| Risk Allele
|
C
|
| P-val
|
2E-8
|
| Odds Ratio
|
4.30 [2.73-5.87] % SD taller
|
[PMID 17186469
] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
[PMID 19030899] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
[PMID 19197348] Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
[PMID 20017971] Assessing the impact of global versus local ancestry in association studies.
[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
] Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
