ADCY5, adenylate cyclase 5, 111

N. diseases: 16; N. variants: 16
Source: GWASCAT ×
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: rs11708067
rs11708067 		0.882 0.080 3 123346931 intron variant A/G snv 0.19
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.840 0.875 4 2010 2018
dbSNP: rs11708067
rs11708067 		0.882 0.080 3 123346931 intron variant A/G snv 0.19
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 4 2010 2019
dbSNP: rs11717195
rs11717195 		1.000 0.080 3 123363551 intron variant T/C snv 0.19
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 1.000 2 2012 2014
dbSNP: rs9883204
rs9883204 		3 123377973 intron variant T/A;C snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.800 1.000 2 2010 2013
dbSNP: rs11708067
rs11708067 		0.882 0.080 3 123346931 intron variant A/G snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2012 2012
dbSNP: rs2877716
rs2877716 		3 123375604 intron variant T/C snv 0.76
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0.800 1.000 1 2010 2010
dbSNP: rs2877716
rs2877716 		3 123375604 intron variant T/C snv 0.76
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 1 2012 2012
dbSNP: rs10934646
rs10934646 		3 123365694 intron variant A/G snv 0.26
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11708067
rs11708067 		0.882 0.080 3 123346931 intron variant A/G snv 0.19
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs11708067
rs11708067 		0.882 0.080 3 123346931 intron variant A/G snv 0.19
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11714441
rs11714441 		3 123440099 intron variant C/T snv 0.40
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs11714441
rs11714441 		3 123440099 intron variant C/T snv 0.40
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11719201
rs11719201 		3 123349897 intron variant C/T snv 0.20
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs11720108
rs11720108 		1.000 0.080 3 123350211 intron variant C/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12330631
rs12330631 		3 123370987 intron variant C/T snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs17295246
rs17295246 		3 123386874 intron variant G/A;C snv 0.19
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2062432
rs2062432 		3 123359232 intron variant G/A snv 0.43
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2062432
rs2062432 		3 123359232 intron variant G/A snv 0.43
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2062432
rs2062432 		3 123359232 intron variant G/A snv 0.43
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2062432
rs2062432 		3 123359232 intron variant G/A snv 0.43
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2877716
rs2877716 		3 123375604 intron variant T/C snv 0.76
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs4093840
rs4093840 		1.000 0.040 3 123358195 intron variant T/A snv 0.41
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs59107033
rs59107033 		3 123386796 intron variant C/G;T snv
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs72964564
rs72964564 		3 123335923 intron variant A/C snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7614016
rs7614016 		3 123351579 intron variant G/A snv 0.19
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018