Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10865035 1.000 0.080 2 100219272 intron variant A/G snv 0.42 2
rs643955 1.000 0.080 8 10033744 intron variant T/A;G snv 1
rs6886392 1.000 0.080 5 100800161 intergenic variant G/C snv 0.27 1
rs55849330 1.000 0.080 5 100848943 intron variant C/A snv 0.23 1
rs7925662 1.000 0.080 11 101537575 intron variant T/C snv 0.26 1
rs4522865 0.882 0.240 4 101794731 intron variant G/A;T snv 4
rs10028805 0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
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
rs4637409 1.000 0.080 4 101832251 intron variant A/G snv 0.27 1
rs4426778 1.000 0.080 4 101859567 intron variant G/A;C snv 1
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs4622329 1.000 0.080 12 101928157 intron variant G/A snv 0.46 1
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
rs11681718 1.000 0.080 2 102434684 non coding transcript exon variant A/G snv 0.22 1
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3093030 0.925 0.120 19 10286727 non coding transcript exon variant C/T snv 0.34 6
rs4917385 1.000 0.080 10 103243964 upstream gene variant T/G snv 0.74 1
rs7258015 0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs11085725 0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs8108236 0.925 0.120 19 10355156 intron variant G/A snv 9.3E-02 2
rs11085727 1.000 0.080 19 10355447 intron variant C/T snv 0.24 1