Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs1246946 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 4
rs4761496 0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23 4
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs1412115 0.925 0.080 10 33799125 regulatory region variant T/C snv 0.58 2
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 2
rs35324266 1.000 0.040 6 32625467 upstream gene variant C/T snv 0.16 1
rs62209647 1.000 0.040 20 33917852 upstream gene variant G/C snv 4.4E-02 1
rs6791479 1.000 0.040 3 189487243 intergenic variant T/A snv 0.48 1
rs7097008 1.000 0.040 10 67849782 non coding transcript exon variant C/A snv 0.60 1
rs9557210 1.000 0.040 13 99395250 intergenic variant G/A snv 0.16 1
rs9651495 1.000 0.040 10 89172624 regulatory region variant G/A snv 0.13 1
rs774121564
ACP1
1.000 0.040 2 275197 missense variant C/G snv 4.1E-06 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
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
rs117984432
ANKRD11
1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02 1
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17