Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1658319 10 79165257 intron variant T/C snv 0.81 1
rs1815314 10 79169036 intron variant G/A;C;T snv 1
rs780151 10 79171724 intron variant G/A snv 0.32 1
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 1
rs1250557 1.000 0.080 10 79306017 intron variant G/T snv 0.63 1
rs1250569 0.925 0.040 10 79285450 intron variant T/C snv 0.44 0.51 1
rs12571751 0.925 0.120 10 79182874 intron variant A/G snv 0.46 1
rs753270 1.000 0.080 10 79205218 intron variant T/A;C snv 1
rs34204798 1.000 0.080 10 79191374 intron variant G/-;GG;GGG;GGGG delins 1
rs703980 1.000 0.080 10 79184084 intron variant G/A snv 0.39 1
rs703972 1.000 0.080 10 79193069 intron variant G/A;C snv 1
rs1250566 10 79286696 intron variant G/A snv 0.24 1
rs1782645 1.000 0.080 10 79288854 intron variant C/A;T snv 1
rs1250542 1.000 0.080 10 79274913 intron variant G/A snv 0.32 1
rs7914926 10 79170941 intron variant A/G snv 0.41 1
rs703984 10 79181660 intron variant G/C;T snv 1
rs704010 0.851 0.080 10 79081391 intron variant T/C snv 0.71 1
rs1268974 1.000 0.080 10 79092621 intron variant A/G snv 0.65 1
rs2802372 10 79287818 intron variant A/C snv 0.44 1
rs10128264 1.000 0.120 10 79200216 intron variant T/C snv 0.64 1
rs74142329 10 79190231 intron variant C/T snv 4.9E-02 1
rs77911174 0.925 0.080 10 79067076 intron variant A/G snv 5.4E-02 1
rs7916441 10 79165820 intron variant G/C snv 0.39 2
rs779933 10 79158760 intron variant G/A snv 0.36 2
rs11593576 0.925 0.040 10 79256139 intron variant C/T snv 0.29 2