Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137853140 0.925 0.200 7 92235531 missense variant G/C snv 2
rs267607203 0.925 0.200 7 92222870 stop gained G/A;C snv 4.0E-06 2
rs267607204 0.925 0.200 7 92234451 stop gained G/T snv 2
rs10151332 1.000 14 99722950 3 prime UTR variant C/T snv 3.2E-05; 0.48 0.41 1
rs137853139 1.000 7 92236488 missense variant T/C snv 1
rs9823731 1.000 3 30641799 intron variant A/G snv 0.66 1
rs117153070 1.000 11 102834237 intron variant G/A snv 1.8E-02 1