CRTAP, cartilage associated protein, 10491

N. diseases: 66; N. variants: 15
Disease: Major Depressive Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4478037
rs4478037
Entrez Id: 10491
Gene Symbol: CRTAP
CRTAP
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. 29317602 2018