Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 9
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 5
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 4
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 4
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 2
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs2179920 1.000 0.040 6 33091097 downstream gene variant C/T snv 0.27 1
rs140361050
ABCC11
1.000 0.040 16 48230493 synonymous variant C/T snv 2.3E-04; 4.0E-06 2.3E-04 1
rs1403821912
ADRA1A
1.000 0.040 8 26864422 missense variant C/T snv 4.0E-06 1
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 9
rs863225281
ALK
0.776 0.200 2 29220829 missense variant G/C;T snv 9
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 8
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 6
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 1
rs779318085
ALK
1.000 0.040 2 29193849 missense variant A/C snv 8.0E-06 4.2E-05 1
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 6
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1315148641
APOBEC1
1.000 0.040 12 7654617 missense variant T/C snv 4.0E-06 2
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 2
rs533748068
ARHGEF2 ; MIR6738
0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5