rs763443434, BRIP1

N. diseases: 2
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 J
141 1.000 0.120 17 61684041 frameshift variant -/GTCAAGCT delins 2.1E-05 0.700 1.000 2 2010 2011
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 1.000 0.120 17 61684041 frameshift variant -/GTCAAGCT delins 2.1E-05 0.700 1.000 1 2008 2008