Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10692845 2 21070463 regulatory region variant -/GA;GACTCAAAGTACACATTTCCTAGA delins 0.69 1
rs11291804 17 30305102 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTTTTTT delins 1
rs11636917 15 63501674 non coding transcript exon variant T/C snv 0.25 1
rs116435220 1 46425014 regulatory region variant C/T snv 8.9E-03 1
rs116961202 8 58469752 regulatory region variant A/G snv 2.9E-02 1
rs117087731 4 72830992 intergenic variant A/T snv 1
rs11745603 5 156967507 upstream gene variant C/G;T snv 1
rs11899121 2 20168212 intergenic variant G/C snv 0.50 1
rs12306094 12 68593375 intergenic variant G/A;C snv 1
rs12320328 12 25255530 upstream gene variant A/G snv 0.11 1
rs12517431 5 156965237 upstream gene variant C/G;T snv 1
rs12677676 8 125490284 intron variant A/G snv 0.20 1
rs1326543 6 53632424 downstream gene variant A/G snv 0.23 1
rs13300056 9 19212562 intergenic variant C/T snv 6.4E-02 1
rs140402167 19 11278037 intergenic variant G/A;T snv 1.1E-02 1
rs143132975 2 21212951 intergenic variant A/T snv 0.50 1
rs144188464 8 86169166 intergenic variant A/G;T snv 4.6E-02 1
rs1456465 1 2895249 intergenic variant G/A;T snv 1
rs147010738 13 72193030 intergenic variant -/GT;GTGT ins 1
rs1470121 3 142906936 intergenic variant G/A snv 0.27 1
rs1568749 3 874399 intergenic variant T/C snv 0.20 1
rs2758886 6 39283061 regulatory region variant G/A;C snv 1
rs28635570 8 125494390 intron variant C/T snv 0.16 1
rs287354 13 68665820 intergenic variant A/G snv 0.61 1
rs287474 13 68701828 intergenic variant T/A snv 0.58 1