DPF3, double PHD fingers 3, 8110

N. diseases: 20; N. variants: 9
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: rs4903064
rs4903064 		0.925 0.120 14 72812712 intron variant T/C snv 0.23
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.710 1.000 2 2017 2019
dbSNP: rs74884082
rs74884082 		1.000 0.080 14 72782711 intron variant C/T snv 0.26
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs10140566
rs10140566 		14 72665482 intron variant T/A;G snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs12887388
rs12887388 		1.000 0.040 14 72863136 intron variant G/A snv 0.64
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.700 1.000 1 2018 2018
dbSNP: rs202075571
rs202075571 		14 72835096 intron variant C/A;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs202075571
rs202075571 		14 72835096 intron variant C/A;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs61986330
rs61986330 		14 72847742 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs6574100
rs6574100 		14 72856974 intron variant A/T snv 0.44
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7160830
rs7160830 		0.925 0.040 14 72673030 intron variant C/G;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs7160830
rs7160830 		0.925 0.040 14 72673030 intron variant C/G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10129954
rs10129954 		1.000 0.040 14 72683993 intron variant C/T snv 0.49
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.020 1.000 2 2018 2018
dbSNP: rs10129954
rs10129954 		1.000 0.040 14 72683993 intron variant C/T snv 0.49
CUI: C0004509
Disease: Azoospermia
Azoospermia 		Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4903064
rs4903064 		0.925 0.120 14 72812712 intron variant T/C snv 0.23
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017