Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1223231582 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs111033565 0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 11
rs111033566 0.742 0.280 7 142750600 missense variant A/C;T snv 11
rs267606982 0.742 0.120 7 142751938 missense variant GC/AT mnv 11
rs777418530 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs10273639 0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
rs61734659 0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 8
rs748405415 0.790 0.160 7 142773993 stop gained G/A;T snv 8
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6
rs773891125
LPL
0.827 0.120 8 19955896 frameshift variant CT/- delins 6
rs12688220 0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5
rs7057398 0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs497078 0.925 0.040 1 15440540 synonymous variant C/A;T snv 3.7E-03; 9.1E-02 2
rs752688735 0.925 0.040 7 142752547 missense variant G/A snv 2