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: rs1331776405
rs1331776405 		2 24827609 splice acceptor variant C/T snv
CUI: C4693522
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19 		0.700 0
dbSNP: rs1553329804
rs1553329804 		2 24820052 frameshift variant G/- delins
CUI: C4693522
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19 		0.700 0
dbSNP: rs1553333167
rs1553333167 		2 24824537 splice acceptor variant C/T snv
CUI: C4693522
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19 		0.700 0
dbSNP: rs750852737
rs750852737 		2 24820011 inframe deletion AAG/- delins 4.0E-06; 2.4E-05 1.4E-05
CUI: C4693522
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19 		0.700 0
dbSNP: rs754914420
rs754914420 		2 24839960 frameshift variant C/-;CC delins
CUI: C4693522
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19 		0.700 0
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: rs1127568
rs1127568 		1.000 0.080 2 24823221 synonymous variant T/C;G snv 0.69; 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2010 2010
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