Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 12
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 11
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10
rs17011141
LINC02257
0.776 0.080 1 221939292 intron variant A/G snv 0.21 10
rs6678517
LAMC1
0.776 0.080 1 183033504 intron variant A/G;T snv 10
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs12143541
TTC22
0.790 0.080 1 54782179 intron variant A/G snv 0.11 9
rs201395236
EFCAB2
0.790 0.080 1 245018119 intron variant T/C snv 1.5E-04 9
rs2184857
LOC105373224
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45 9
rs3753366
GNG12
0.790 0.080 1 67729450 intron variant C/G snv 0.20 9
rs4546885
LAMC1
0.790 0.080 1 183056420 intron variant G/A;C snv 9
rs658191
MACF1
0.790 0.080 1 39458103 non coding transcript exon variant C/G snv 6.1E-02 9
rs6658977 0.790 0.080 1 221876478 downstream gene variant G/T snv 0.29 9
rs6691195 0.790 0.080 1 221989031 downstream gene variant C/A snv 0.19 9
rs72647484 0.790 0.080 1 22261235 regulatory region variant T/C snv 6.2E-02 9
rs7528276
MACF1
0.790 0.080 1 39344315 intron variant T/A;C snv 9
rs7542665
L1TD1
0.790 0.080 1 62207365 missense variant T/C snv 0.63 0.67 9
rs137853200
EPHA2
0.925 0.120 1 16129440 missense variant G/A snv 2
rs139787163
EPHA2
0.925 0.120 1 16125271 missense variant C/T snv 4.8E-04 3.6E-04 2