ADCY3, adenylate cyclase 3, 109

N. diseases: 47; N. variants: 32
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: rs6545800
rs6545800
2 24896016 intron variant C/T snv 0.53
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 4 2015 2019
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 3 2015 2017
dbSNP: rs10203386
rs10203386
2 24913997 intron variant T/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2019 2019
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 2 2015 2016
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 2 2015 2017
dbSNP: rs6545814
rs6545814
2 24908447 intron variant A/G snv 0.53
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 2 2012 2014
dbSNP: rs6545814
rs6545814
2 24908447 intron variant A/G snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2012 2014
dbSNP: rs6545814
rs6545814
2 24908447 intron variant A/G snv 0.53
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 2 2012 2014
dbSNP: rs10198275
rs10198275
2 24907673 intron variant A/C snv 0.53
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs10200566
rs10200566
2 24907593 intron variant T/G snv 0.54
CUI: C0562350
Disease: Hip circumference
Hip circumference
0.700 1.000 1 2019 2019
dbSNP: rs10203482
rs10203482
2 24914047 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs10206196
rs10206196
2 24914454 intron variant T/C snv 0.55
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs11125803
rs11125803
2 24829308 intron variant C/T snv 0.68
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0562350
Disease: Hip circumference
Hip circumference
0.700 1.000 1 2015 2015
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0011334
Disease: Dental caries
Dental caries
Stomatognathic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2012 2012
dbSNP: rs13035244
rs13035244
2 24911140 intron variant T/C snv 0.53
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2019 2019
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs13407913
rs13407913
0.827 0.120 2 24874775 intron variant A/G snv 0.54
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1529897
rs1529897
2 24863958 intron variant T/A;G snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1550115
rs1550115
1.000 0.040 2 24818751 intron variant C/T snv 0.69
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs35609705
rs35609705
2 24868853 intron variant AA/-;A;AAA;AAAA delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.700 1.000 1 2016 2016