rs10052657, PDE4D

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.700 1.000 1 2011 2011
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.700 1.000 1 2011 2011
Squamous cell carcinoma of esophagus
329 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.700 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.010 1.000 1 2018 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.010 1.000 1 2018 2018
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
1158 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.700 1.000 1 2018 2018
Adolescent idiopathic scoliosis
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
1178 0.807 0.120 5 59111944 intron variant C/A snv 0.17 0.700 1.000 1 2018 2018