Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12885300 0.790 0.200 14 80211923 5 prime UTR variant C/A;G;T snv 7
rs1306185959 0.851 0.040 8 38429805 missense variant T/C snv 7.0E-06 4
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1320938886 0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs1340827343 0.851 0.040 6 31165259 missense variant C/T snv 4
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1381537616 0.851 0.040 7 27174132 missense variant C/T snv 4
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs1453633223 0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs149840192 0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1957106 0.851 0.040 14 35404564 synonymous variant G/A snv 0.28 0.25 4
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs200187877 0.851 0.040 4 23795829 missense variant C/T snv 8.0E-06 7.0E-06 4
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2017309 0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs2234248 0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5