Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063537 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3818292 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs805304 0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182