MOXD1, monooxygenase DBH like 1, 26002

N. diseases: 10; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9373014
rs9373014
Entrez Id: 26002
Gene Symbol: MOXD1
MOXD1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs589756
rs589756
Entrez Id: 26002
Gene Symbol: MOXD1
MOXD1
CUI: C0424678
Disease:
Lean body mass 		A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs589756
rs589756
Entrez Id: 26002
Gene Symbol: MOXD1
MOXD1
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs6901304
rs6901304
Entrez Id: 26002
Gene Symbol: MOXD1
MOXD1
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009