Source: GWASCAT

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: rs3764419
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2013
dbSNP: rs62070648
rs62070648
ATAD5
17 30883577 intron variant G/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs11080134
rs11080134
ATAD5
17 30834485 missense variant A/G snv 0.27 0.25
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11080134
rs11080134
ATAD5
17 30834485 missense variant A/G snv 0.27 0.25
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs143663961
rs143663961
ATAD5
1.000 0.120 17 30854202 intron variant -/T delins
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs17826219
rs17826219
ATAD5
17 30834827 missense variant G/A snv 0.13 0.10
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs3764419
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs62070648
rs62070648
ATAD5
17 30883577 intron variant G/A;C snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs7223535
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs7223535
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7223535
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs7223535
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs74815160
rs74815160
ATAD5
17 30830140 upstream gene variant A/T snv 0.18
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9890032
rs9890032
ATAD5
17 30838916 intron variant C/G snv 0.49
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2018 2018