Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10737670 1.000 0.040 1 196388616 intron variant A/C;G snv 0.27 2
rs10754187 1.000 0.040 1 196447122 intron variant A/G;T snv 2
rs10801530 1.000 0.040 1 196392367 intron variant G/T snv 0.27 2
rs10801531 1.000 0.040 1 196394414 intron variant G/A snv 0.27 2
rs10801532 1.000 0.040 1 196395046 intron variant A/G;T snv 2
rs10801537 1.000 0.040 1 196457711 intron variant A/G snv 0.33 2
rs10922071 1.000 0.040 1 196464740 intron variant G/A snv 0.33 2
rs11807331 1.000 0.040 1 196458681 intron variant T/C snv 0.33 2
rs12065463 1.000 0.040 1 196495624 intron variant T/C snv 0.33 2
rs12069983 1.000 0.040 1 196418611 intron variant C/A snv 0.27 2
rs12069990 1.000 0.040 1 196418679 intron variant C/T snv 0.27 2
rs12729649 1.000 0.040 1 196418502 intron variant G/A snv 0.61 2
rs1538687 1.000 0.040 1 196428645 intron variant C/T snv 0.62 2
rs1769996 1.000 0.040 1 196383911 intron variant C/T snv 0.64 2
rs2878557 1.000 0.040 1 196433643 intron variant T/C snv 0.61 2
rs3855964 1.000 0.040 1 196414986 intron variant T/G snv 0.70 2
rs3927686 1.000 0.040 1 196416519 intron variant T/C snv 0.70 2
rs3928857 1.000 0.040 1 196414471 intron variant T/C snv 0.64 2
rs7535696 1.000 0.040 1 196402302 intron variant T/C snv 0.27 2
rs10754196 1.000 0.040 1 196601576 intron variant A/G snv 0.30 1
rs10754198 1.000 0.040 1 196604375 intron variant A/T snv 0.30 1
rs10922082 1.000 0.040 1 196544564 intron variant G/A snv 0.30 1
rs10922083 1.000 0.040 1 196547268 intron variant C/A;T snv 1
rs10922084 1.000 0.040 1 196556184 intron variant A/C snv 0.30 1
rs16840224 1.000 0.040 1 196600551 intron variant C/T snv 0.27 1