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: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
Hereditary Breast and Ovarian Cancer Syndrome
0.700 1.000 3 2002 2015
dbSNP: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
0.700 1.000 3 2002 2019
dbSNP: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
PANCREATIC CANCER, SUSCEPTIBILITY TO, 4
0.700 0
dbSNP: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.700 0
dbSNP: rs80358189
rs80358189
0.827 0.200 17 43074522 splice acceptor variant C/A;G;T snv 1.2E-05
FANCONI ANEMIA, COMPLEMENTATION GROUP S
0.700 0