MEOX2, mesenchyme homeobox 2, 4223

N. diseases: 29; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs740567
rs740567
Entrez Id: 4223;101927524
Gene Symbol: MEOX2;LINC02587
MEOX2;LINC02587
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019