Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519893 0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs711830 0.882 0.120 2 176172583 3 prime UTR variant A/C;G;T snv 0.76 3
rs6755777 0.882 0.120 2 176178498 non coding transcript exon variant T/A;G snv 3
rs752590 1.000 0.040 2 113215368 intron variant A/G snv 0.27 2
rs320203 1.000 0.040 9 102180944 intergenic variant C/A snv 0.17 1
rs688187 1.000 0.040 19 39242112 upstream gene variant G/A snv 0.39 1
rs1337040042 1.000 0.040 17 81131085 start lost T/C snv 1
rs773301216 1.000 0.040 7 91118066 missense variant G/A snv 4.0E-06 1.4E-05 1
rs755711267 1.000 0.040 4 75607279 missense variant C/T snv 3.6E-05 2.8E-05 1
rs753734841 1.000 0.040 2 27440906 missense variant C/T snv 1.2E-05 1.4E-05 1
rs375029799 1.000 0.040 2 178776873 missense variant C/T snv 2.4E-05 2.1E-05 1
rs200212150 1.000 0.040 12 40314084 missense variant G/A;T snv 1.6E-05 1.4E-05 1
rs144052967 1.000 0.040 9 36665552 missense variant C/T snv 1.3E-04 6.3E-05 1
rs112071820 1.000 0.040 3 139130268 intron variant -/GATTCAGAATCCA delins 0.30 1
rs1423134583 1.000 0.040 10 26096393 missense variant T/A snv 4.0E-06 1
rs201821707 1.000 0.040 3 27346152 missense variant G/A;C;T snv 3.4E-04; 6.0E-05; 4.0E-06 1
rs72831838 1.000 0.040 2 113258824 non coding transcript exon variant C/G;T snv 1
rs374535834 1.000 0.040 11 67435048 missense variant C/A;T snv 4.1E-06; 6.5E-05 1
rs746238409
RYK
1.000 0.040 3 134202791 missense variant C/T snv 2.8E-05 2.1E-05 1
rs368877591 1.000 0.040 3 43348090 missense variant G/A snv 5.9E-05 1.4E-05 1
rs762000831 1.000 0.040 2 219483170 missense variant C/T snv 8.9E-05 1.4E-05 1
rs113498671 1.000 0.040 3 195884972 missense variant C/T snv 8.0E-06 1
rs370624303 1.000 0.040 12 131910720 missense variant G/A snv 3.2E-05 2.1E-05 1
rs200610853 1.000 0.040 7 141724247 missense variant G/A snv 4.0E-06 7.0E-06 1