Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116046827
BSN
0.827 0.120 3 49618715 intron variant T/C snv 8.6E-03 5
rs11614178 0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs11616188 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 5
rs11624293 0.827 0.120 14 88022477 intron variant T/C snv 0.13 5
rs11649613 0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 5
rs11675538 0.827 0.120 2 65459327 intron variant C/T snv 0.29 5
rs11691685 0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs11749040 0.827 0.120 5 40396323 regulatory region variant G/A snv 0.15 5
rs11749391 0.827 0.120 5 150849504 intron variant T/C snv 0.21 5
rs11750385 0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs1182188 0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs12075255 0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs12131796 0.827 0.120 1 200909599 intron variant G/A snv 0.22 5
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12369214 0.807 0.120 12 106804833 intron variant G/A snv 0.41 6
rs1250573 0.827 0.120 10 79282718 intron variant G/A snv 0.23 5
rs12694846 0.827 0.120 2 230283413 intron variant A/G snv 0.20 5
rs12718244 0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs12879003 0.827 0.120 14 35359535 downstream gene variant T/A;G snv 0.43 5
rs1292035 0.827 0.120 17 59912196 intron variant G/A snv 0.16 5
rs12932970 0.827 0.120 16 85970504 intron variant T/C snv 0.29 5
rs12943464 0.827 0.120 17 47612985 intron variant A/T snv 0.45 5
rs12968719 0.827 0.120 18 12879467 intron variant G/A snv 8.5E-02 6
rs12987977 0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs13107612 0.827 0.120 4 101818823 intron variant C/T snv 0.31 5