MC4R, melanocortin 4 receptor, 4160

N. diseases: 149; N. variants: 58
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: rs121913564
rs121913564
0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.800 1.000 5 2003 2015
dbSNP: rs1016862
rs1016862
1.000 0.040 18 60371844 missense variant A/C snv
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs121913564
rs121913564
0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs121913564
rs121913564
0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs121913559
rs121913559
1.000 0.080 18 60372045 missense variant A/C;G snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.710 1.000 1 2005 2005
dbSNP: rs1057517991
rs1057517991
0.925 0.120 18 60371539 missense variant A/G snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.720 1.000 2 2003 2008
dbSNP: rs1057517991
rs1057517991
0.925 0.120 18 60371539 missense variant A/G snv 4.0E-06
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs151102515
rs151102515
1.000 0.080 18 60371940 missense variant A/G snv 2.4E-05 2.8E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 1999 1999
dbSNP: rs368264587
rs368264587
1.000 0.080 18 60371467 missense variant A/G snv 1.2E-05 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs746906443
rs746906443
0.925 0.080 18 60371868 missense variant A/G snv 4.0E-06
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs746906443
rs746906443
0.925 0.080 18 60371868 missense variant A/G snv 4.0E-06
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs13447337
rs13447337
1.000 0.080 18 60371400 missense variant A/G snv 8.0E-06 7.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs193922685
rs193922685
1.000 0.080 18 60371812 missense variant A/G snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs376439188
rs376439188
1.000 0.080 18 60372189 missense variant A/G snv 4.0E-06 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs756232889
rs756232889
1.000 0.080 18 60371512 missense variant A/G snv 4.0E-06 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs79783591
rs79783591
1.000 0.080 18 60371544 missense variant A/T snv 1.0E-03 1.1E-04
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.710 1.000 1 2020 2020
dbSNP: rs772393451
rs772393451
1.000 0.080 18 60371601 missense variant A/T snv 1.6E-05 7.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs121913557
rs121913557
1.000 0.080 18 60372202 missense variant C/A;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.710 1.000 1 2009 2009
dbSNP: rs121913562
rs121913562
1.000 0.080 18 60371538 missense variant C/A;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.800 0
dbSNP: rs1267063448
rs1267063448
1.000 0.080 18 60372131 missense variant C/G snv 4.0E-06 7.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2229616
rs2229616
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.100 1.000 13 1999 2014
dbSNP: rs747681609
rs747681609
1.000 0.080 18 60371856 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.700 1.000 8 2000 2014
dbSNP: rs13447333
rs13447333
0.925 0.120 18 60371808 missense variant C/T snv 1.6E-05
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs187152753
rs187152753
1.000 0.080 18 60371593 missense variant C/T snv 5.6E-05 1.3E-04
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.810 1.000 1 2007 2007
dbSNP: rs2229616
rs2229616
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008