Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs1790349 0.882 0.040 11 71431304 intron variant T/C snv 0.19 4
rs5880 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10
rs763802417 0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs1866389 0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs1408888 0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs3732581 0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs532019808 0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs6700896 0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs6850 0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs9818870 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9