CADM2, cell adhesion molecule 2, 253559

N. diseases: 58; N. variants: 96
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: rs2325036
rs2325036
3 85770262 intron variant A/C snv 0.41
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2015 2015
dbSNP: rs35344466
rs35344466
3 85583871 intron variant A/C snv 0.17
CUI: C0027769
Disease: Nervousness
Nervousness
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6807666
rs6807666
1.000 0.040 3 85545278 intron variant A/C snv 0.59
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6804845
rs6804845
1.000 0.040 3 85514696 intron variant A/C;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs13078807
rs13078807
0.925 0.120 3 85835000 intron variant A/G snv 0.15
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 2 2010 2013
dbSNP: rs13078807
rs13078807
0.925 0.120 3 85835000 intron variant A/G snv 0.15
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 2 2010 2013
dbSNP: rs10511083
rs10511083
1.000 0.040 3 85521809 intron variant A/G snv 0.51
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs13078807
rs13078807
0.925 0.120 3 85835000 intron variant A/G snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2010 2010
dbSNP: rs13078807
rs13078807
0.925 0.120 3 85835000 intron variant A/G snv 0.15
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs13078807
rs13078807
0.925 0.120 3 85835000 intron variant A/G snv 0.15
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1368748
rs1368748
1.000 0.040 3 85363180 intron variant A/G snv 0.50
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs17023019
rs17023019
1.000 0.040 3 85565122 intron variant A/G snv 0.59
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs17791975
rs17791975
3 85068884 intron variant A/G snv 7.9E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator
0.700 1.000 1 2015 2015
dbSNP: rs17791975
rs17791975
3 85068884 intron variant A/G snv 7.9E-03
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs1872556
rs1872556
3 85016078 intron variant A/G snv 0.74
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs2035562
rs2035562
3 85007370 intron variant A/G snv 0.74
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2018 2018
dbSNP: rs34495106
rs34495106
3 85601986 intron variant A/G snv 0.51
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs3901898
rs3901898
1.000 0.040 3 85853881 intron variant A/G snv 0.71
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs5023755
rs5023755
3 85628643 intron variant A/G snv 0.32
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs62261676
rs62261676
3 85649427 intron variant A/G snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs62263923
rs62263923
1.000 0.040 3 85625640 intron variant A/G snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs62263923
rs62263923
1.000 0.040 3 85625640 intron variant A/G snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7627287
rs7627287
1.000 0.040 3 85863363 intron variant A/G snv 0.36
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7632056
rs7632056
1.000 0.040 3 85609875 intron variant A/G snv 0.52
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs917346005
rs917346005
0.925 0.080 3 85912502 missense variant A/G snv
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015