Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs77542162 1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147233090 0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs7385804 0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs2413450 22 37074184 intron variant T/C snv 0.61 5
rs62160676 2 111410354 intron variant T/C;G snv 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs9483788 6 135114363 intergenic variant T/C snv 0.19 3
rs1331309 6 135085040 intron variant T/G snv 0.19 2