Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs80358721 0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 14
rs1799950 0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs1256031 0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs1256030 0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs121913322 0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs185229225 0.851 0.120 4 13607505 intron variant T/C snv 4
rs2073495
LTF
0.851 0.200 3 46439467 missense variant C/A;G snv 4.9E-04; 0.33 4
rs495139 0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs9110
LTF
0.851 0.200 3 46439310 missense variant A/C;G;T snv 0.39 0.40 4
rs121964872 0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3