CDH13, cadherin 13, 1012

N. diseases: 205; N. variants: 47
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: rs4783244
rs4783244 		0.925 0.120 16 82628663 intron variant G/T snv 0.38
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.800 1.000 3 2011 2014
dbSNP: rs12051272
rs12051272 		0.925 0.120 16 82629683 intron variant G/C;T snv
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.800 1.000 2 2012 2012
dbSNP: rs8057927
rs8057927 		1.000 0.040 16 82659207 intron variant T/C snv 0.12
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs9940464
rs9940464 		1.000 0.040 16 83327170 intron variant T/C snv 0.39
CUI: C0024530
Disease: Malaria
Malaria 		Infections 0.800 1.000 1 2013 2013
dbSNP: rs7500448
rs7500448 		1.000 0.040 16 83012185 intron variant A/G snv 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 4 2017 2018
dbSNP: rs7206608
rs7206608 		16 82839023 intron variant C/G snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs7500448
rs7500448 		1.000 0.040 16 83012185 intron variant A/G snv 0.20
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2019
dbSNP: rs10492862
rs10492862 		1.000 0.040 16 82833851 intron variant C/A;G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs11149581
rs11149581 		16 83583973 intron variant T/G snv 0.27
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs114132812
rs114132812 		1.000 0.040 16 83784283 intron variant A/T snv 5.4E-03
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2016 2016
dbSNP: rs115067260
rs115067260 		1.000 0.040 16 83788697 intron variant A/T snv 1.0E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11864066
rs11864066 		16 83353167 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12597537
rs12597537 		16 82637031 intron variant A/G snv 8.1E-02
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs12598815
rs12598815 		16 82814603 intron variant A/G snv 4.9E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs12598815
rs12598815 		16 82814603 intron variant A/G snv 4.9E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs12599599
rs12599599 		16 82636934 intron variant G/A snv 3.4E-02
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs140186760
rs140186760 		1.000 0.080 16 82961263 intron variant G/A snv 7.4E-03
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		Male Urogenital Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1489313
rs1489313 		1.000 0.040 16 83423986 intron variant C/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs16957913
rs16957913 		16 82636644 intron variant T/C snv 3.7E-02
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs181710595
rs181710595 		16 83433739 intron variant A/G;T snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs2194285
rs2194285 		0.925 0.040 16 82861212 intron variant G/A snv 0.74
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2194285
rs2194285 		0.925 0.040 16 82861212 intron variant G/A snv 0.74
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs3096277
rs3096277 		16 83730599 intron variant T/C snv 0.74
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2007 2007
dbSNP: rs3096277
rs3096277 		16 83730599 intron variant T/C snv 0.74
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2007 2007
dbSNP: rs4075464
rs4075464 		16 83115081 intron variant A/G snv 0.57
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018