rs28897672, BRCA1

N. diseases: 16
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.
FANCONI ANEMIA, COMPLEMENTATION GROUP S
28 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 0
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 0
PANCREATIC CANCER, SUSCEPTIBILITY TO, 4
22 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 0
Hereditary Breast and Ovarian Cancer Syndrome
2117 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 1.000 34 1994 2013
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1
2277 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 1.000 8 1998 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.020 1.000 2 1998 2011
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.020 1.000 2 1998 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.870 1.000 12 2004 2019
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.770 1.000 7 2005 2019
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.700 1.000 11 2006 2017
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.030 1.000 3 2006 2010
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.730 1.000 3 2006 2010
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.730 1.000 3 2006 2010
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.010 1.000 1 2008 2008
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.010 1.000 1 2008 2008
Malignant tumor of peritoneum
CUI: C0153467
Disease: Malignant tumor of peritoneum
1 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.010 1.000 1 2016 2016