Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs186696265 0.882 0.040 6 160690668 intergenic variant C/T snv 1.0E-02 6
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs12290663 0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02 2
rs144972973 0.925 0.040 15 44272494 intergenic variant A/G snv 1.8E-02 2
rs149232047 0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04 2
rs16999497 0.925 0.040 X 129601222 regulatory region variant T/C snv 7.8E-02 2
rs189889864 0.925 0.040 9 104634643 downstream gene variant G/A snv 2.8E-03 2
rs192427471 0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03 2
rs201394051 0.925 0.040 5 117697919 intergenic variant TA/-;TATA;TATATA delins 2
rs62568141 0.925 0.040 9 77012344 regulatory region variant C/T snv 2.4E-02 2
rs9295128 0.925 0.040 6 160330499 intergenic variant G/T snv 1.1E-02 2
rs113681054 1.000 0.040 12 21250045 intergenic variant T/C snv 0.18 1
rs140104968 1.000 0.040 7 99946004 intron variant C/T snv 1.5E-02 1
rs140607780 1.000 0.040 7 100505900 upstream gene variant G/A snv 1.0E-02 1
rs62471956 1.000 0.040 7 99823462 upstream gene variant G/A snv 3.4E-02 1
rs559110055
ABCA1
0.925 0.160 9 104840491 missense variant A/G snv 4.0E-06 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14