Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 10
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 4
rs7717457 5 40887679 intergenic variant A/G snv 0.23 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs765189442
ABCB11
0.925 0.080 2 168995422 missense variant T/C snv 8.1E-06 4
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs61573157
ADAMTS14
0.882 0.160 10 70760503 missense variant C/T snv 8.6E-02 7.5E-02 6
rs12774070
ADAMTS14
0.925 0.120 10 70753879 missense variant C/A;G snv 0.23 0.19 4
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs201745983
ALDH2
0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 12
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42