Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74142329 10 79190231 intron variant C/T snv 4.9E-02 1
rs753270 1.000 0.080 10 79205218 intron variant T/A;C snv 1
rs77911174 0.925 0.080 10 79067076 intron variant A/G snv 5.4E-02 1
rs779933 10 79158760 intron variant G/A snv 0.36 2
rs780151 10 79171724 intron variant G/A snv 0.32 1
rs780159 10 79147390 intron variant A/C;G snv 2
rs7914926 10 79170941 intron variant A/G snv 0.41 1
rs7916441 10 79165820 intron variant G/C snv 0.39 2