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
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs2165241 0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs3825942 0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 15
rs74315329 0.732 0.240 1 171636338 stop gained G/A snv 1.1E-03 8.7E-04 15
rs11258194 0.776 0.160 10 13110400 missense variant T/A snv 4.4E-02 6.0E-02 9
rs10120688 0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs7049105 0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs199746824 0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 6
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 4
rs1052990 0.882 0.040 7 116508316 3 prime UTR variant T/C;G snv 3
rs1333037 0.925 0.040 9 22040766 intron variant C/T snv 0.71 3
rs7037117 0.882 0.040 9 117721385 3 prime UTR variant A/G snv 0.40 3
rs284491 0.925 0.040 8 104946405 intron variant C/T snv 0.45 2