Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13149359 0.776 0.080 4 94017467 intergenic variant C/A snv 0.29 10
rs13204733 0.776 0.080 6 55701310 intergenic variant A/G snv 0.10 10
rs1427760 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 10
rs145364999
CHD1
0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 10
rs1512436 0.790 0.080 11 106436144 intergenic variant T/C snv 0.50 10
rs16878812
LOC112267956 ; FKBP5
0.776 0.080 6 35601785 intron variant A/G snv 0.15 10
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 10
rs17011141
LINC02257
0.776 0.080 1 221939292 intron variant A/G snv 0.21 10
rs17035310 0.790 0.080 4 105143597 upstream gene variant C/T snv 0.14 10
rs17094983
LINC01500
0.776 0.080 14 58722643 intron variant G/A snv 0.12 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs1741640
LAMA5
0.776 0.080 20 62357358 intron variant T/C snv 0.66 10
rs17503919
RNGTT
0.790 0.080 6 88856018 intron variant A/G snv 9.4E-02 10
rs17806780
ZNF827
0.790 0.080 4 145811502 intron variant T/C snv 0.18 10
rs17816465
FMN1
0.776 0.080 15 32864185 intron variant G/A snv 0.15 10
rs189583 0.776 0.080 20 6395810 regulatory region variant G/C;T snv 10
rs1924816 0.776 0.080 13 73423824 intron variant A/G snv 0.29 10
rs1963413
TMEM91 ; B9D2
0.776 0.080 19 41365668 intron variant G/A;C;T snv 10
rs2052678
TMTC1
0.790 0.080 12 29680396 intron variant G/A snv 0.21 10
rs2186607
TRPC6
0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 10
rs2250430
PLEKHG6
0.776 0.080 12 6312008 intron variant A/C;T snv 10
rs2293581
GREM1 ; LOC100131315
0.776 0.080 15 32718535 5 prime UTR variant G/A;C snv 0.27 10
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 10
rs2427308
CABLES2
0.790 0.080 20 62394395 intron variant C/T snv 0.22 10