Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113017087
rs113017087
APC
1 1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 0.010 1.000 1 2016 2016
dbSNP: rs115658307
rs115658307
APC
1 1.000 0.040 5 112707537 5 prime UTR variant C/T snv 4.8E-03 0.010 1.000 1 2016 2016
dbSNP: rs138386816
rs138386816
APC
1 1.000 0.040 5 112707566 5 prime UTR variant C/T snv 7.2E-03 0.010 1.000 1 2016 2016
dbSNP: rs75612255
rs75612255
APC
1 1.000 0.040 5 112737543 intron variant T/C snv 0.010 1.000 1 2016 2016