Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 2
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 2
rs10002268 1.000 0.080 4 55653725 intergenic variant T/C snv 0.41 1
rs12542990 1.000 0.080 8 81122216 intergenic variant G/C snv 0.32 1
rs17028375 1.000 0.080 2 64085008 downstream gene variant T/C snv 0.11 1
rs6123557 1.000 0.080 20 56232196 intergenic variant C/T snv 0.21 1
rs7726463 1.000 0.080 5 37954971 intron variant T/C snv 9.1E-02 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs748676559
ACACA
0.925 0.080 17 37284932 missense variant C/T snv 4.0E-06 2.1E-05 3
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs11066008
ACAD10
1.000 0.080 12 111702865 intron variant A/G snv 9.1E-03 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
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
rs4646776
ALDH2
0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03 2
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36