Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34