Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs4576506 0.925 0.120 9 31546474 intergenic variant A/G snv 0.91 2
rs753129 0.925 0.120 4 55802265 downstream gene variant A/G snv 0.23 2
rs10207628
BIN1
0.925 0.120 2 127094445 intron variant G/A;C snv 2
rs4038131
VSNL1
0.925 0.120 2 17593765 intron variant A/G snv 0.12 2
rs3849810 1.000 0.080 8 52097046 intergenic variant A/C;T snv 1
rs549656827 1.000 0.080 5 35349326 intergenic variant G/A snv 6.9E-03 1
rs75459873 1.000 0.080 1 23929822 downstream gene variant G/A snv 3.2E-02 1
rs10994278
ANK3
1.000 0.080 10 60249461 intron variant T/C snv 0.11 1