Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 1
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 1
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3