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.
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.776 0.280 10 102876898 intron variant G/C;T snv 0.700 1.000 1 2018 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2018 2018
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2018 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of urinary bladder
316 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2009 2009
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2015 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2009 2009
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.776 0.280 10 102876898 intron variant G/C;T snv 0.010 1.000 1 2017 2017