Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 2
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3
rs11082011
CELF4
0.925 0.040 18 37565159 intron variant C/T snv 0.53 3
rs2984618
TAL1
0.925 0.040 1 47224766 intron variant G/T snv 0.52 1
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 2
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 1
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2