Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs2241715 0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs367597251 0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6
rs1234220 0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs230530 0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs779555087 0.882 0.080 20 44414561 missense variant A/G snv 1.6E-05 1.4E-05 3
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs5854292 0.851 0.080 3 168680960 intron variant AA/-;A;AAA delins 5
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56