Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 8
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7313833 0.851 0.120 12 27930263 intergenic variant G/A snv 0.37 4
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 4
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3
rs4954956 0.882 0.120 2 138787007 regulatory region variant C/T snv 0.25 3
rs67397200 0.827 0.160 19 17290595 upstream gene variant C/G snv 0.27 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
rs7748275 0.882 0.120 6 3580855 downstream gene variant T/A snv 8.2E-02 2
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2229109
ABCB1
0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs35068177
ABCB1
0.882 0.120 7 87550213 synonymous variant T/C snv 2.2E-04 3.1E-04 3
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 93
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 36
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 13
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22