rs1799943, BRCA2

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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 0.020 0.500 2 2012 2014
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 0.010 1 2016 2016
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 0.010 1 2016 2016