Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 2
rs11621969 0.925 0.040 14 75347325 intergenic variant T/C snv 0.14 2
rs11800854 0.925 0.040 1 233584238 intergenic variant G/A snv 0.11 2
rs13145041 0.925 0.040 4 189616909 intergenic variant A/C;G;T snv 2
rs13237474 0.925 0.040 7 135816721 intron variant C/T snv 2.3E-02 2
rs1370967 0.925 0.040 5 111203694 intergenic variant G/A snv 7.8E-02 2
rs1932040 0.925 0.040 6 45729051 TF binding site variant A/G snv 0.69 2
rs1953021 0.925 0.040 9 12914397 intergenic variant G/T snv 0.69 2
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs7086701 0.925 0.040 10 10298081 intergenic variant G/A;T snv 2
rs7567687 0.925 0.040 2 129276753 upstream gene variant C/T snv 0.43 2
rs9984417 0.925 0.040 21 22474790 intergenic variant A/T snv 0.52 2
rs11634042
ADAMTS7 ; MORF4L1
0.882 0.120 15 78813008 intron variant C/T snv 0.33 4
rs3826782
ADGRE1
0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs17879146
BIRC5
0.925 0.040 17 78223864 3 prime UTR variant T/G snv 1.2E-02 1.2E-02 2
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs25681
C5
0.882 0.120 9 121017727 synonymous variant G/A snv 0.47 0.35 3
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3