Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892151 1.000 11 117661016 intron variant C/T snv 9.7E-02 3
rs1048412 1.000 6 30064718 3 prime UTR variant A/G snv 0.15 0.17 1
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
rs1433591886 1.000 2 169633213 missense variant G/A snv 4.0E-06 1
rs3740996 1.000 11 5680051 missense variant G/A snv 0.13 0.10 1
rs4657412 1.000 1 165207796 intron variant G/A snv 0.79 1
rs57302492 1.000 2 70831099 missense variant T/A snv 7.0E-02 8.9E-02 1
rs749569169 1.000 7 29512676 missense variant A/G snv 4.0E-06 1
rs756151230 1.000 7 92470377 missense variant G/C snv 1
rs774027752 1.000 19 40845472 missense variant T/C snv 8.0E-06 1.4E-05 1
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
rs1799972 0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs11881222 0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs11045819 0.851 0.120 12 21176879 missense variant C/A;T snv 0.11; 4.0E-06 4
rs4619915 0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 7
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs3921 0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8