Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 11
rs2107538
LOC105371744 ; CCL5
0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10