Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494334 1.000 0.080 1 163535374 intergenic variant G/A snv 0.10 1
rs1867898 1.000 0.080 2 133762000 intergenic variant G/A snv 0.22 1
rs1986513 1.000 0.080 4 125146073 intergenic variant A/T snv 8.9E-02 1
rs4791746 1.000 0.080 17 8723039 intergenic variant T/A;C snv 1
rs9384169 1.000 0.080 6 153992036 intergenic variant T/C snv 0.36 1
rs9478495 1.000 0.080 6 154002774 intergenic variant G/A snv 0.19 1
rs965972 1.000 0.080 1 193494720 intron variant G/A snv 0.86 1
rs768020372 1.000 0.080 12 111792761 missense variant C/G;T snv 6.3E-06 1
rs2270162 1.000 0.080 7 69596980 intron variant C/G;T snv 1
rs2288156 1.000 0.080 17 8741536 missense variant C/A;T snv 4.0E-06; 8.8E-02 1
rs255105 1.000 0.080 7 30692491 intron variant T/C snv 0.50 1
rs778052047 1.000 0.080 7 50528268 missense variant C/T snv 4.0E-06 1
rs4648319 1.000 0.080 11 113443641 intron variant G/A;T snv 1
rs780737633
F2R
1.000 0.080 5 76733086 synonymous variant G/A;C snv 4.0E-06; 4.0E-06 1
rs1978340 1.000 0.080 2 170813611 non coding transcript exon variant G/A snv 0.25 1
rs769395 1.000 0.080 2 170860293 3 prime UTR variant G/A snv 0.76 1
rs5376 1.000 0.080 18 77268853 missense variant G/A snv 0.98 0.91 1
rs950302 1.000 0.080 1 167114567 intron variant A/G snv 0.47 1
rs3104703 1.000 0.080 16 9971279 intron variant T/G snv 0.48 1
rs3219790 1.000 0.080 16 10183568 upstream gene variant CACACACACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACACA delins 1
rs767749 1.000 0.080 16 9754614 3 prime UTR variant T/G snv 0.81 1
rs17189632 1.000 0.080 9 101605720 intron variant T/A snv 0.41 1
rs274618 1.000 0.080 7 86642700 upstream gene variant T/A;C snv 1
rs11606194 1.000 0.080 11 113910259 intron variant T/C snv 6.1E-02 1
rs363332 1.000 0.080 10 117243156 intron variant G/A snv 0.18 1