Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs4416670 0.827 0.240 6 43982716 intergenic variant T/C snv 0.45 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs908867 0.851 0.160 11 27724217 intron variant C/G;T snv 7
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs3916966 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 4
rs4305745 0.882 0.080 6 132572573 downstream gene variant G/A snv 0.55 4
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1922242
ABCB1
0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs143830698
ACE
0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 4