Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1424847607
EPHA2
1.000 0.080 1 16133591 missense variant A/G snv 4.0E-06 1
rs376894109
PRKCZ
1.000 0.080 1 2175293 missense variant C/T snv 4.0E-06 7.0E-06 1
rs539738963
STK40
1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 1
rs755089893
STK40
1.000 0.080 1 36355378 missense variant A/G snv 4.0E-06; 8.0E-06 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs11692435
ACTR1B
0.790 0.080 2 97658891 missense variant G/A snv 7.0E-02 6.7E-02 10
rs11884596
LOC105373831
0.776 0.080 2 198747683 intron variant T/C snv 0.32 10
rs3731861
PNKD ; CATIP-AS2
0.776 0.080 2 218326533 intron variant T/C snv 0.32 10
rs448513
TANC1
0.776 0.080 2 159108040 intron variant T/C snv 0.41 10
rs983402 0.776 0.080 2 198916862 intron variant T/C snv 0.62 10
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs11893063
LOC105373831
0.790 0.080 2 198737201 intron variant G/A snv 0.37 9
rs13020391
LOC105373881 ; PNKD
0.790 0.080 2 218319713 intron variant C/T snv 0.32 9
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 9
rs2901879 0.790 0.080 2 66738934 intergenic variant C/T snv 0.54 9
rs4849303
ACOXL
0.790 0.080 2 110970905 intron variant C/G;T snv 9
rs4954585 0.790 0.080 2 136240824 intergenic variant C/G;T snv 9
rs6720296
LINC01121
0.790 0.080 2 45181130 intron variant A/C snv 0.52 9
rs7593422 0.790 0.080 2 199266972 downstream gene variant A/T snv 0.41 9
rs7606512
LINC01173
0.790 0.080 2 234701030 intron variant C/T snv 0.11 9
rs7606562
PPP1R21
0.790 0.080 2 48459556 intron variant T/A;C snv 9
rs63751127
MSH6 ; FBXO11
0.882 0.200 2 47800177 stop gained C/A;T snv 4.0E-06; 4.0E-06 5
rs149061352
TTN
1.000 0.080 2 178785717 missense variant G/A;T snv 4.4E-05; 4.0E-06 1
rs751398376
TTN ; TTN-AS1
1.000 0.080 2 178609836 missense variant C/A;G snv 1.2E-05; 4.0E-06 1