Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7544735 1.000 0.040 1 220825571 intron variant G/A snv 0.22 3
rs10489202 0.925 0.080 1 167933841 intron variant G/T snv 0.20 2
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs11265022 1.000 0.040 1 158542829 downstream gene variant T/A snv 0.21 2
rs12094989 1.000 0.040 1 26521895 upstream gene variant C/T snv 0.29 2
rs16840314 1.000 0.040 1 158547563 synonymous variant G/A snv 0.23 0.19 2
rs2241107 1.000 0.040 1 156212919 upstream gene variant T/C;G snv 2
rs2253677 1.000 0.040 1 156201505 intron variant C/G snv 0.42 2
rs2297141 0.925 0.080 1 85581241 non coding transcript exon variant G/A;C snv 2
rs2785663 1.000 0.040 1 157650968 intergenic variant T/G snv 0.64 2
rs2853641 1.000 0.040 1 156211979 3 prime UTR variant A/G snv 0.43 2
rs6576776 0.925 0.080 1 85584394 downstream gene variant C/A;G snv 2
rs6670311 1.000 0.040 1 26538994 intron variant C/G snv 4.4E-02 2
rs863344 1.000 0.040 1 158565041 intron variant G/A snv 0.19 2
rs863345 0.925 0.080 1 158565192 intron variant C/T snv 0.54 2
rs10399681 1.000 0.040 1 158555761 upstream gene variant G/A snv 0.50 1
rs10429895 1.000 0.040 1 190689509 intron variant C/T snv 0.32 1
rs10489573 1.000 0.040 1 18358708 intron variant C/T snv 0.21 1
rs10489676 1.000 0.040 1 157650099 intergenic variant T/C snv 0.24 1
rs10493240 1.000 0.040 1 58318478 intron variant G/C;T snv 1
rs10493241 1.000 0.040 1 58318299 intron variant G/A snv 0.13 1
rs10493249 1.000 0.040 1 58306455 intron variant G/T snv 0.14 1
rs10493260 1.000 0.040 1 59112910 intron variant T/C snv 0.11 1
rs10494164 1.000 0.040 1 114003906 intron variant A/G snv 6.7E-02 1
rs10494229 1.000 0.040 1 119686494 intron variant A/G snv 0.23 1