Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115092681 1.000 0.080 3 174201323 intron variant G/A;C;T snv 2
rs141864436 1.000 0.080 2 50971652 intron variant G/A snv 1.6E-02 2
rs57504626 1.000 0.080 19 19609590 intron variant C/T snv 0.10 2
rs112284299 1.000 0.080 3 179850308 intron variant G/C snv 1.6E-02 2
rs6693796 1.000 0.080 1 170674137 intron variant T/C snv 7.7E-02 2
rs143838781 1.000 0.080 12 113940539 intron variant G/A snv 7.0E-03 2
rs75639901 1.000 0.080 6 25667803 intron variant A/G snv 4.8E-02 2
rs2631781 1.000 0.080 1 76128101 intron variant C/A;T snv 2
rs58847779 1.000 0.080 22 37736644 intron variant T/C snv 4.4E-02 2
rs7810240 1.000 0.080 7 150387372 intron variant T/C;G snv 2
rs13064411 3 113327793 synonymous variant A/G snv 0.12 9.9E-02 1
rs16914931 9 98330034 intron variant G/A snv 0.10 1