rs143969848, None

N. diseases: 4
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.
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.925 0.160 3 36958902 TF binding site variant G/A snv 9.8E-03 0.010 1.000 1 2018 2018
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.925 0.160 3 36958902 TF binding site variant G/A snv 9.8E-03 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.925 0.160 3 36958902 TF binding site variant G/A snv 9.8E-03 0.010 1.000 1 2018 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.925 0.160 3 36958902 TF binding site variant G/A snv 9.8E-03 0.010 1.000 1 2018 2018