Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10211550 1.000 0.040 2 197518575 intron variant G/T snv 0.37 2
rs1024582 1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10520163 1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs10791097 1.000 0.040 11 130848735 intron variant T/G snv 0.60 2
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11191419 1.000 0.040 10 102852578 intron variant T/A snv 0.36 2
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs11191582 1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02 2
rs112209031 1.000 0.040 6 32524630 intron variant T/C;G snv 2
rs113397282 1.000 0.040 6 32520273 intron variant T/C;G snv 2
rs114086406 1.000 0.040 6 32374760 intron variant G/A snv 2
rs114274203 1.000 0.040 6 31300843 intron variant C/T snv 2
rs114277634 1.000 0.040 6 31474954 intron variant T/A;C snv 2
rs114455101 1.000 0.040 6 32465853 intron variant T/G snv 2
rs114838832 1.000 0.040 6 30937536 intron variant A/G snv 2
rs114875775 1.000 0.040 6 32521255 intron variant A/T snv 1.8E-02 2
rs114963521 1.000 0.040 6 30791080 intron variant C/T snv 2
rs115035678 1.000 0.040 6 32381780 intron variant A/T snv 2
rs115052633 1.000 0.040 6 31621487 intron variant C/G;T snv 2
rs115123779 1.000 0.040 6 29510044 intron variant G/A;C;T snv 2