Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 4
rs7839488
SNTB1
0.882 0.040 8 120550178 intron variant G/A snv 0.47 4
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
rs9318086
MIPEP
0.882 0.040 13 23858328 intron variant A/G snv 0.55 3
rs577948
MIR100HG
0.882 0.040 11 122159482 intron variant A/G snv 0.33 3
rs6469937
SNTB1
0.882 0.040 8 120598198 intron variant G/A snv 0.48 3
rs1656966 0.925 0.080 3 186748463 intron variant G/A snv 0.18 2
rs999556 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 2
rs16872571
CLNK
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 2
rs872863
DENND1A
0.925 0.160 9 123392075 intron variant C/T snv 9.4E-02 2
rs2089760
LAMA1
0.925 0.040 18 7118956 upstream gene variant C/T snv 0.43 2
rs10747502
LOC100129620
1.000 0.040 1 99058491 intron variant A/G snv 0.86 2
rs10053502 1.000 0.040 5 39979070 intron variant C/T snv 6.9E-02 1
rs11618212 1.000 0.040 13 105444463 intergenic variant A/G snv 0.18 1
rs11838472 1.000 0.040 13 73167012 regulatory region variant C/T snv 0.12 1
rs12216812 1.000 0.040 8 81239512 upstream gene variant G/A snv 6.2E-02 1
rs12525668 1.000 0.040 6 107696467 downstream gene variant A/G snv 6.6E-02 1
rs1559777 1.000 0.040 15 57788419 intergenic variant G/A snv 0.28 1
rs17822114 1.000 0.040 16 60699699 intergenic variant C/T snv 3.4E-02 1
rs189798 1.000 0.040 8 9133067 downstream gene variant A/G snv 0.70 1
rs4737395 1.000 0.040 8 55686989 intergenic variant G/A;C snv 1
rs4839680 1.000 0.040 3 144183185 downstream gene variant T/C snv 2.4E-02 1
rs6472235 1.000 0.040 8 65909795 intergenic variant T/G snv 0.46 1
rs6857559 1.000 0.040 4 188199757 intergenic variant T/C snv 0.63 1