rs16941, BRCA1

N. diseases: 7
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 Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.020 1.000 2 2004 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.020 1.000 2 2004 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.010 1.000 1 2004 2004
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.010 1.000 1 2004 2004
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.010 1.000 1 2014 2014
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 0.010 1.000 1 2018 2018