Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10336 0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048412 1.000 6 30064718 3 prime UTR variant A/G snv 0.15 0.17 1
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs10892151 1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs11045819 0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11881222 0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs1188975135 0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs1194919682 0.925 0.040 2 136115158 missense variant A/G snv 2
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1272938495 1.000 2 136115225 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1276738522 1.000 12 6232664 start lost A/G snv 4.9E-06 1
rs1292288729 1.000 19 41009375 missense variant T/C snv 7.4E-06 1
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs1433591886 1.000 2 169633213 missense variant G/A snv 4.0E-06 1
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799972 0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121