Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6671633 1.000 0.040 1 45034622 intron variant A/G snv 0.59 1
rs6678726 1.000 0.040 1 45030723 intron variant A/G;T snv 1
rs909406 1.000 0.040 16 3099517 upstream gene variant C/T snv 0.47 1
rs3739028 1.000 0.040 2 135150276 intron variant T/C snv 3.7E-02 1
rs10407807 1.000 0.040 19 19935293 3 prime UTR variant C/A snv 8.4E-02 1
rs10411195 1.000 0.040 19 19925367 intron variant T/C snv 8.0E-02 1
rs11786 1.000 0.040 19 19935409 3 prime UTR variant C/T snv 9.3E-02 1
rs12610295 1.000 0.040 19 19928158 intron variant C/A snv 0.15 1
rs2335367 1.000 0.040 19 19913057 intron variant T/C snv 0.96 1
rs4809014 1.000 0.040 19 19944193 intron variant G/A;C snv 1
rs7250793 1.000 0.040 19 19925055 intron variant T/C snv 0.88 1
rs11563346 1.000 0.040 7 127368435 intron variant A/G snv 0.13 1
rs11563463 1.000 0.040 7 127366874 intron variant C/T snv 0.32 1
rs11563634 1.000 0.040 7 127367715 intron variant C/G snv 0.15 1
rs2285337 1.000 0.040 7 127367931 intron variant G/A snv 0.16 1
rs2285338 1.000 0.040 7 127368376 intron variant C/A;G snv 0.64 1
rs17815373 1.000 0.040 19 56097531 intron variant G/A snv 0.15 1
rs562907 1.000 0.040 19 56100455 intron variant G/A;T snv 1
rs685117 1.000 0.040 19 56111849 intron variant G/A;C snv 0.85 1
rs8103672 1.000 0.040 19 56119948 intron variant G/A;C snv 1
rs11672966 1.000 0.040 19 23095699 intron variant G/A snv 6.1E-02 1
rs1473419 1.000 0.040 19 23101548 intron variant C/T snv 0.54 1
rs1693286 1.000 0.040 19 23096201 intron variant C/A;G;T snv 0.15 1
rs1693294 1.000 0.040 19 23094893 intron variant C/A;T snv 1
rs2035172 1.000 0.040 19 23121702 intron variant T/C snv 0.12 1