CAPN15, calpain 15, 6650

N. diseases: 6; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		0.100 GeneticVariation phenotype GWASCAT GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. 31164008 2019
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.100 GeneticVariation disease GWASCAT GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. 31164008 2019
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0.100 GeneticVariation phenotype GWASDB GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.100 GeneticVariation phenotype GWASCAT GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863 2013
CUI: C0086543
Disease: Cataract
Cataract 		0.010 Biomarker disease BEFREE SOLH is a candidate gene for CATM (hereditary cataracts with microphthalmia), which maps in this region. 9722942 1998
CUI: C0521707
Disease: Bilateral cataracts (disorder)
Bilateral cataracts (disorder) 		0.010 Biomarker disease BEFREE SOLH is a candidate gene for CATM (hereditary cataracts with microphthalmia), which maps in this region. 9722942 1998