Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs398090202
rs398090202
ADCY3 ; LOC105377626
2 24833715 intron variant -/A delins
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4077678
rs4077678
ADCY3
2 24899971 intron variant C/G snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs55701159
rs55701159
ADCY3
2 24916727 intron variant T/G snv 0.11
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs56073414
rs56073414
ADCY3
2 24911142 intron variant C/A snv 8.0E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6725517
rs6725517
ADCY3
1.000 0.080 2 24906604 intron variant A/G snv 0.51
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs6737082
rs6737082
ADCY3
2 24915171 intron variant A/C snv 0.56
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs7586879
rs7586879
ADCY3
2 24894108 intron variant C/T snv 0.47
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs7586879
rs7586879
ADCY3
2 24894108 intron variant C/T snv 0.47
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs7586879
rs7586879
ADCY3
2 24894108 intron variant C/T snv 0.47
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs7945
rs7945
ADCY3 ; CENPO
2 24819753 3 prime UTR variant A/G snv 0.17
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs1331776405
rs1331776405
ADCY3
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
ADCY3 ; CENPO
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
ADCY3
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
ADCY3 ; CENPO
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
ADCY3
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