Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2300206 0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs2974935 0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs481519 0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 18
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs73110464 0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs75316749 0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 18
rs7725218 0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31