Source: ALL

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: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2011 2011
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.700 1.000 1 2014 2014
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.700 1.000 1 2011 2011
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs10052657
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018