rs80359014, BRCA2

N. diseases: 10
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 breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.320 13 32362596 missense variant A/G;T snv 0.800 0
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 1.000 14 2000 2018
Hereditary Breast and Ovarian Cancer Syndrome
2117 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 1.000 12 2000 2018
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
2633 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 1.000 7 2007 2015
FANCONI ANEMIA, COMPLEMENTATION GROUP D1
37 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0
GLIOMA SUSCEPTIBILITY 3
CUI: C2751641
Disease: GLIOMA SUSCEPTIBILITY 3
22 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0
PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
21 0.763 0.320 13 32362596 missense variant A/G;T snv 0.700 0