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: rs3803915
rs3803915
AP3D1
1.000 0.080 19 2160530 intron variant C/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.800 1.000 1 2015 2015
dbSNP: rs57908212
rs57908212
AP3D1
19 2161322 intron variant T/C snv 0.46
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs12985850
rs12985850
AP3D1
19 2155043 intron variant G/A snv 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs183203602
rs183203602
AP3D1
19 2154724 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs25673
rs25673
AP3D1
0.925 0.040 19 2109158 missense variant T/C;G snv 0.12; 4.8E-04
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs25673
rs25673
AP3D1
0.925 0.040 19 2109158 missense variant T/C;G snv 0.12; 4.8E-04
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs35917214
rs35917214
AP3D1
19 2135715 intron variant T/G snv 6.4E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4807203
rs4807203
AP3D1
19 2127273 intron variant A/G snv 0.32
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs57908212
rs57908212
AP3D1
19 2161322 intron variant T/C snv 0.46
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs57908212
rs57908212
AP3D1
19 2161322 intron variant T/C snv 0.46
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7249081
rs7249081
AP3D1
19 2157168 intron variant T/C;G snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs7249081
rs7249081
AP3D1
19 2157168 intron variant T/C;G snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019