Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16