NMU, neuromedin U, 10874

N. diseases: 68; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs149106723
rs149106723
1.000 0.080 4 55599178 missense variant G/A snv 1.6E-05 4.2E-05
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2006 2009
dbSNP: rs12500837
rs12500837
1.000 0.080 4 55627872 intron variant T/C snv 0.21
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6827359
rs6827359
1.000 0.080 4 55627773 intron variant T/C snv 0.49
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs9999653
rs9999653
1.000 0.080 4 55632082 intron variant C/T snv 0.51
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017