Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 9
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs147061479 1.000 0.040 8 65264756 intergenic variant C/T snv 1.9E-02 1
rs6554759 1.000 0.040 5 1316987 downstream gene variant G/A snv 0.85 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs201963
ADAM18
1.000 0.040 8 39721376 intron variant A/C snv 1
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 3
rs34988193
ANKDD1A
1.000 0.040 15 64943580 missense variant A/G snv 0.31 0.28 2
rs117677079
ANXA5
0.882 0.040 4 121673909 intron variant T/C snv 8.3E-03 3
rs1131239
ANXA5
1.000 0.040 4 121696590 5 prime UTR variant G/A;C;T snv 0.12 0.17 1
rs145619195
ANXA5
1.000 0.040 4 121674585 intron variant T/C snv 9.4E-04 1
rs2306415
ANXA5
1.000 0.040 4 121696476 intron variant C/G snv 0.16 1
rs2306420
ANXA5
1.000 0.040 4 121670320 intron variant G/A snv 0.21 1
rs41278075
ANXA5
1.000 0.040 4 121669758 intron variant G/A snv 0.23 0.18 1
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9