rs180177092, PALB2

N. diseases: 5
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.851 0.280 16 23635788 frameshift variant AG/- delins 0.700 1.000 11 2007 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.851 0.280 16 23635788 frameshift variant AG/- delins 0.700 1.000 4 2007 2015
FANCONI ANEMIA, COMPLEMENTATION GROUP N
CUI: C1835817
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP N
13 0.851 0.280 16 23635788 frameshift variant AG/- delins 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.851 0.280 16 23635788 frameshift variant AG/- delins 0.700 0
PANCREATIC CANCER, SUSCEPTIBILITY TO, 3
CUI: C3150547
Disease: PANCREATIC CANCER, SUSCEPTIBILITY TO, 3
14 0.851 0.280 16 23635788 frameshift variant AG/- delins 0.700 0