Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2294020 0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs7665090 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6