Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs41526548 1.000 0.080 9 92129496 upstream gene variant T/C snv 1
rs1394871591
ABCA1
0.827 0.200 9 104903619 missense variant G/C snv 4.8E-06 5
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs767425642
ACE
0.882 0.120 17 63489010 missense variant G/A;T snv 3.2E-05; 4.0E-06 3
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs748703149
APOE
0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6