Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10243383 1.000 0.040 7 22242733 intron variant C/T snv 0.51 2
rs114969316 1.000 0.040 6 88460643 intergenic variant A/G snv 1.6E-02 2
rs115319209 1.000 0.040 14 75298968 downstream gene variant G/A snv 1.0E-02 2
rs12036147 1.000 0.040 1 239835413 intron variant A/G;T snv 2
rs141980369 1.000 0.040 6 118888344 intron variant G/A snv 6.1E-02 2
rs142383097 1.000 0.040 1 10461101 3 prime UTR variant A/C;G snv 2.0E-02 2
rs143916815 1.000 0.040 15 39191714 intron variant G/C snv 1.0E-02 2
rs35426224 1.000 0.040 14 99783354 intron variant G/A snv 5.2E-02 2
rs59711329 1.000 0.040 19 57901128 intron variant G/A;C snv 2
rs6487668 1.000 0.040 12 9200312 intron variant C/A snv 0.78 2
rs734152 1.000 0.040 12 109759971 intron variant G/C;T snv 2
rs76782312
AK9
1.000 0.040 6 109643865 intron variant C/T snv 1.6E-02 2
rs7897478 1.000 0.040 10 29945955 intergenic variant A/C;G snv 2
rs9432230 1.000 0.040 1 230882365 intron variant C/T snv 6.4E-02 2
rs9487114 1.000 0.040 6 109460597 intron variant T/C;G snv 2