Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs1860561
ATP2A2
0.851 0.080 12 110345436 intron variant G/A snv 0.19 5
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs243864
MMP2
0.925 0.080 16 55478410 intron variant T/G snv 0.19 3
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs1009388
POMC
1.000 0.040 2 25168232 intron variant G/C snv 0.18 1
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs6684209
CASQ2
1.000 0.040 1 115707991 intron variant C/T snv 0.17 2
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs3212247
RIPK3
0.925 0.040 14 24340589 upstream gene variant A/G snv 0.12 2
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs17859821
MMP2
1.000 0.040 16 55478141 intron variant G/A;C snv 0.11 2
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs6787362
FRMD4B
0.925 0.040 3 69178228 intron variant A/G snv 9.3E-02 2
rs2276109
MMP12
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs2230345
GRK5
0.807 0.160 10 119326585 missense variant A/T snv 3.8E-02 9.0E-02 6
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6