Source: ALL
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: rs10065633
rs10065633
1 1.000 0.040 5 132481024 intron variant T/C snv 0.38 0.010 1.000 1 2008 2008
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: rs1416364034
rs1416364034
1 1.000 0.040 17 42300731 missense variant G/A snv 4.0E-06 0.010 1.000 1 2004 2004
dbSNP: rs1444068378
rs1444068378
1 1.000 0.040 2 105363404 missense variant G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs75612255
rs75612255
APC
1 1.000 0.040 5 112737543 intron variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs774164690
rs774164690
1 1.000 0.040 7 50400428 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs923941004
rs923941004
1 1.000 0.040 9 5078334 missense variant T/C snv 0.010 1.000 1 2015 2015
dbSNP: rs6413463
rs6413463
1 1.000 0.040 9 21970990 missense variant A/G;T snv 2.9E-05; 3.0E-04 0.700 0
dbSNP: rs10931910
rs10931910
2 0.925 0.040 2 200659013 intron variant A/G;T snv 0.010 < 0.001 1 2014 2014
dbSNP: rs1258094111
rs1258094111
2 0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs17886724
rs17886724
2 0.925 0.040 17 42344145 intron variant A/G snv 0.35 0.010 1.000 1 2012 2012
dbSNP: rs201045130
rs201045130
2 0.925 0.040 1 39659467 missense variant A/G snv 9.9E-05 1.0E-04 0.010 1.000 1 2016 2016
dbSNP: rs201820837
rs201820837
2 0.925 0.040 12 11869532 missense variant G/A;T snv 2.4E-05; 6.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs587782006
rs587782006
2 0.925 0.040 17 7673761 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs7090445
rs7090445
2 0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 0.010 1.000 1 2019 2019
dbSNP: rs754894156
rs754894156
2 0.925 0.040 21 34834544 missense variant C/T snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs765669662
rs765669662
2 0.925 0.040 8 85465317 missense variant G/A;T snv 2.0E-05; 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs947141826
rs947141826
2 0.925 0.040 10 133394281 missense variant C/T snv 2.1E-05 0.010 1.000 1 1993 1993
dbSNP: rs10405859
rs10405859
3 0.882 0.080 19 45099523 intron variant T/C snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs121909629
rs121909629
3 0.882 0.200 8 38415905 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs139834892
rs139834892
3 0.882 0.040 19 43553481 missense variant C/T snv 6.4E-05 1.1E-04 0.010 1.000 1 2018 2018
dbSNP: rs2308950
rs2308950
3 0.882 0.040 1 15507011 missense variant C/G;T snv 4.0E-06; 1.1E-02 0.010 1.000 1 2018 2018
dbSNP: rs6964823
rs6964823
3 0.925 0.040 7 50392398 intron variant G/A snv 0.45 0.010 1.000 1 2019 2019