Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10209110 1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs11123810 0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11123811 1.000 0.120 2 100143710 intron variant T/C snv 0.55 1
rs6712515 0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs9653442 1.000 0.120 2 100208905 intron variant C/T snv 0.46 2
rs1160542 1.000 0.120 2 100215693 intron variant G/A snv 0.45 1
rs34619498 1.000 0.120 4 100505575 intron variant T/C snv 2.3E-02 1
rs3775369 1.000 0.120 4 100512097 intron variant G/A snv 3.8E-02 1
rs3783613 0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs16910526 0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs10275421 1.000 0.120 7 101299780 non coding transcript exon variant G/A snv 7.2E-02 1
rs8029797 1.000 0.120 15 101365954 non coding transcript exon variant T/A;G snv 1
rs678347 1.000 0.120 8 101451374 intron variant G/A;C snv 1
rs646514 1.000 0.120 8 101453833 upstream gene variant C/G;T snv 1
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs12434439 0.925 0.160 14 102068203 upstream gene variant G/C;T snv 2
rs3844283 0.882 0.200 3 10222796 missense variant C/G snv 0.37 0.35 3
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1241312324 0.925 0.200 4 102567083 missense variant T/C snv 4.0E-06 2
rs948138 1.000 0.120 11 102630934 downstream gene variant G/A snv 0.59 1
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38