Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10035291 1.000 0.040 5 81500549 intron variant T/C snv 0.46 1
rs10058613 0.925 0.040 5 138358306 intron variant C/A;G;T snv 2
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1012053 1.000 0.040 13 42079301 intron variant C/A snv 0.85 1
rs10134944 1.000 0.040 14 57652478 intron variant C/T snv 0.13 1
rs10168049 1.000 0.040 2 121320830 intergenic variant A/G snv 0.16 1
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs10275045 0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1042779 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 3
rs10455979 1.000 0.040 6 166581772 intron variant C/A;G;T snv 1
rs10457441 1.000 0.040 6 98124244 intron variant T/A;C snv 2
rs10459221 1.000 0.040 12 49073211 upstream gene variant C/A;G snv 1
rs10488140 1.000 0.040 7 55070695 intron variant C/T snv 0.26 1
rs10489167 1.000 0.040 1 40710794 intron variant G/A snv 0.13 1
rs10489744 0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs10501439 1.000 0.040 11 79374802 intron variant A/G snv 0.18 1
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10509129 1.000 0.040 10 60311283 intron variant G/A;T snv 1
rs10511083 1.000 0.040 3 85521809 intron variant A/G snv 0.51 1
rs10512928 1.000 0.040 5 7546298 intron variant C/T snv 0.15 1
rs10513249 1.000 0.040 9 114541631 intergenic variant C/A;G snv 1
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs105633 0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3