Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736973 1.000 0.040 7 38302014 upstream gene variant A/C snv 0.86 1
rs3811272 1.000 0.040 14 22273851 intron variant C/T snv 0.29 1
rs3853524 1.000 0.040 1 143665797 intergenic variant C/A;T snv 1
rs4726572 1.000 0.040 7 142717016 upstream gene variant C/A snv 7.9E-02 1
rs4982590 1.000 0.040 14 22250515 intron variant G/A snv 0.14 1
rs6462829 1.000 0.040 7 38292616 upstream gene variant C/T snv 0.15 1
rs6464528 1.000 0.040 7 142717058 upstream gene variant G/A snv 3.9E-02 1
rs6572261 1.000 0.040 14 22103621 upstream gene variant C/T snv 8.3E-02 1
rs6572331 1.000 0.040 14 22246958 intron variant G/A snv 0.15 1
rs6572349 1.000 0.040 14 22268365 intron variant C/T snv 0.22 1
rs6572351 1.000 0.040 14 22268415 intron variant C/T snv 0.47 1
rs6673776 1.000 0.040 1 143566021 intron variant T/A;C snv 3.3E-02 1
rs6953248 1.000 0.040 7 38316814 downstream gene variant A/C snv 0.14 1
rs6966279 1.000 0.040 7 38329947 upstream gene variant A/C snv 0.14 1
rs7141113 1.000 0.040 14 22268014 intron variant G/T snv 0.15 1
rs7147975 1.000 0.040 14 22022482 intergenic variant A/G snv 0.48 1
rs7155927 1.000 0.040 14 22263097 intron variant A/G snv 0.23 1
rs718880 1.000 0.040 7 38322398 upstream gene variant G/A snv 0.12 1
rs7272481 1.000 0.040 20 19181915 intergenic variant A/G;T snv 1
rs72990858 1.000 0.040 6 104699909 intergenic variant G/A snv 7.4E-02 1
rs8022578 1.000 0.040 14 22101908 upstream gene variant A/G snv 0.30 1
rs8022710 1.000 0.040 14 22027789 intergenic variant C/A snv 0.71 1
rs979027 1.000 0.040 14 22020269 intergenic variant G/A snv 0.46 1
rs990962 1.000 0.040 14 22099284 downstream gene variant T/C snv 0.16 1
rs9972232 1.000 0.040 14 22269708 intron variant G/A;C snv 1