Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10761731 10 63267850 intron variant A/T snv 0.38 6
rs7896518 10 63344740 intron variant A/G snv 0.38 4
rs10761741 1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs4379723 10 63203689 intron variant T/C snv 0.43 1