Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62096058 1.000 0.040 18 60229853 intergenic variant G/A snv 0.34 1
rs72893199 1.000 0.040 18 37602745 intron variant T/C snv 0.18 1
rs730356 1.000 0.040 2 147779492 intergenic variant T/A snv 0.15 1
rs888415 1.000 0.040 14 74642492 regulatory region variant A/G;T snv 1
rs9966951 1.000 0.040 18 60108063 intergenic variant G/A snv 0.34 1
rs998884 1.000 0.040 2 147782283 intergenic variant A/G snv 0.37 1
rs1017730 1.000 0.040 11 47711942 intron variant G/A snv 0.18 1
rs9671386 1.000 0.040 14 74684344 intron variant G/A snv 0.73 1
rs7152906 1.000 0.040 14 74658837 intron variant T/A;C snv 1
rs79827531 1.000 0.040 2 167752805 regulatory region variant G/A snv 0.14 1
rs56084168 1.000 0.040 17 81110774 3 prime UTR variant C/T snv 0.15 1
rs61731122 1.000 0.040 1 64632626 synonymous variant G/A;T snv 1.8E-02; 4.0E-06 1
rs1368748 1.000 0.040 3 85363180 intron variant A/G snv 0.50 1
rs4856278 1.000 0.040 3 85599499 intron variant A/G;T snv 1
rs62250661 1.000 0.040 3 85402044 intron variant C/A snv 0.38 1
rs62253085 1.000 0.040 3 85344618 intron variant A/G;T snv 1
rs6807666 1.000 0.040 3 85545278 intron variant A/C snv 0.59 1
rs7355953 1.000 0.040 3 85742987 intron variant T/A;C snv 0.16 1
rs818219 1.000 0.040 3 85325439 intron variant T/C snv 0.58 1
rs9811546 1.000 0.040 3 85342522 intron variant G/A snv 0.26 1
rs9828595 1.000 0.040 3 85843897 intron variant T/A;C;G snv 1
rs9837462 1.000 0.040 3 85109415 intron variant C/A snv 0.25 1
rs9861237 1.000 0.040 3 85353319 intron variant T/C snv 0.39 1
rs9870384 1.000 0.040 3 84960666 intron variant C/T snv 0.29 1
rs1539844 1.000 0.040 18 37540169 intron variant G/A snv 0.12 1