Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 7
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5