Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2447182 8 119341744 intergenic variant A/G snv 0.83 1
rs176185
WBP1L
10 102796297 intron variant G/C snv 0.82 1
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs659580
PRRX1
1 170664755 intron variant T/C snv 0.81 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 2
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs4665630
KLHL29
0.925 0.080 2 23675447 intron variant C/T snv 0.78 3
rs11099680
NR3C2
1.000 0.040 4 148182095 intron variant G/A snv 0.78 2
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs180070
LINC01497
0.882 0.040 17 69960745 upstream gene variant G/T snv 0.77 4
rs6677719 1 159753330 intergenic variant C/T snv 0.77 1
rs9907379
LINC02875
17 61412532 non coding transcript exon variant T/C snv 0.74 0.77 1
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs2504778
CD164L2
1 27381490 intron variant G/A snv 0.77 1
rs1808593
NOS3
0.925 0.080 7 151011214 intron variant G/T snv 0.77 3
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 3
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs4496877 7 150983418 intergenic variant T/G snv 0.74 1
rs10501367
APLNR
1.000 0.040 11 57238113 upstream gene variant T/C snv 0.73 2
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73 3
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21