Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6025211 1.000 0.080 20 56864307 intergenic variant C/G;T snv 1
rs649053 1.000 0.080 9 21387419 upstream gene variant A/G;T snv 1
rs7821974 1.000 0.080 8 37592483 downstream gene variant T/C snv 0.22 1
rs8113007 1.000 0.080 19 39252463 upstream gene variant A/T snv 0.29 1
rs878461 1.000 0.080 2 127415841 upstream gene variant T/C;G snv 0.11 1
rs9877457 1.000 0.080 3 135564539 intergenic variant A/G;T snv 1
rs9970827 1.000 0.080 1 185409746 regulatory region variant G/A snv 0.37 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs749574370
ABCB1
0.925 0.080 7 87545934 missense variant T/A;G snv 4.0E-06; 4.0E-06 2
rs201159898
ABCB1
1.000 0.080 7 87549509 missense variant T/A;C snv 1.2E-05 4.9E-05 1
rs28364274
ABCB1
1.000 0.080 7 87504335 missense variant C/T snv 4.7E-03 4.6E-03 1
rs45456698
ABCB1
1.000 0.080 7 87504335 missense variant C/T snv 1
rs66904256
ABCB4
0.882 0.080 7 87439777 missense variant T/A snv 2
rs3740066
ABCC2
0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 25
rs12621038
ACYP2
0.882 0.120 2 54163976 intron variant C/T snv 0.16 3
rs653765
ADAM10
0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
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
rs1014509103
ADAMTS4
1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05 2
rs2830581
ADAMTS5
1.000 0.080 21 26921481 3 prime UTR variant G/A;C snv 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 60
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52