Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3136817
APEX1 ; OSGEP
0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs104894103
APTX
0.807 0.280 9 32974495 stop gained C/G;T snv 4.0E-06; 1.6E-04 6
rs377522479
ARHGAP24
0.882 0.080 4 85931021 missense variant C/T snv 2.0E-05 3.5E-05 4
rs771723690
ARHGAP24
0.882 0.080 4 85570622 synonymous variant G/A snv 1.6E-05 3
rs369576054
ARHGAP24 ; MAPK10
0.807 0.120 4 85994925 missense variant C/T snv 2.8E-05 4.9E-05 6
rs781734330
ATP13A2
0.851 0.080 1 16995981 missense variant C/T snv 4
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs8173
AURKA
0.763 0.240 20 56369735 3 prime UTR variant C/G;T snv 9
rs121964884
AVP
0.851 0.200 20 3083005 stop gained G/A;T snv 4
rs6435862
BARD1
0.827 0.160 2 214807822 intron variant G/A;C;T snv 5
rs3768716
BARD1
0.851 0.080 2 214771070 intron variant T/C snv 0.16 4
rs17487792
BARD1
0.882 0.080 2 214778776 intron variant C/T snv 0.16 3
rs3738888
BARD1
0.882 0.080 2 214730440 missense variant G/A;T snv 8.4E-03 3
rs3768707
BARD1
0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4712653
CASC15
0.882 0.080 6 22125735 intron variant T/C;G snv 3
rs9295536
CASC15
0.882 0.080 6 22131700 intron variant C/A snv 0.58 3