Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs16867253
GRHL1
0.851 0.120 2 9956965 intron variant G/T snv 5.8E-02 7
rs1805217 1.000 0.080 21 9885601 intergenic variant G/A;C snv 1
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs4965430
IGF1R
0.882 0.200 15 98725621 intron variant C/G snv 0.52 3
rs2660304
MIR137HG ; MIR137 ; MIR2682
0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83 2
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs10821415
AOPEP
1.000 0.080 9 94951177 intron variant C/A snv 0.34 1
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs4244285
CYP2C19
0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs7026071
AOPEP
1.000 0.080 9 94730238 intron variant T/A;C snv 1
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs11773884
CDK6
1.000 0.080 7 92655809 intron variant A/G snv 0.36 1
rs56201652
CDK6
1.000 0.080 7 92648802 intron variant G/A snv 0.29 1
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs7632427 0.925 0.160 3 89485227 downstream gene variant T/A;C snv 2
rs6771054
EPHA3
1.000 0.080 3 89440379 intron variant T/A;C;G snv 1
rs4148738
ABCB1
0.925 0.120 7 87533733 intron variant C/T snv 0.62 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs58238559
ABCB4
0.882 0.120 7 87452957 missense variant T/C snv 1.1E-02 9.2E-03 3
rs6907805 1.000 0.080 6 87146285 downstream gene variant G/T snv 0.54 1
rs2031522 1.000 0.080 6 87111783 intergenic variant A/G snv 0.37 1
rs72926475 1.000 0.080 2 86367364 downstream gene variant G/A snv 0.14 1
rs2592551
GGCX
1.000 0.080 2 85553008 synonymous variant G/A snv 0.26 0.30 1
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16