Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs12764899 1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs7085104 1.000 0.040 10 102869116 intron variant A/G snv 0.35 2
rs11191419 1.000 0.040 10 102852578 intron variant T/A snv 0.36 2
rs10883795 1.000 0.040 10 102894820 intron variant T/C snv 0.30 1
rs11191424 1.000 0.040 10 102866129 intron variant G/A snv 0.36 1
rs12244388 1.000 0.040 10 102880295 intron variant G/A;T snv 1