Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs979614 1.000 0.080 6 20661892 intron variant A/G snv 0.35 1
rs9688952 1.000 0.080 6 20741152 intron variant G/A snv 0.38 1
rs9465871 0.882 0.120 6 20717024 intron variant T/C snv 0.30 3
rs9465852 1.000 0.080 6 20641669 intron variant G/A;C snv 1
rs9465850 1.000 0.080 6 20639178 intron variant C/T snv 0.19 1
rs9465847 1.000 0.080 6 20634197 intron variant G/T snv 0.19 1
rs9465846 1.000 0.080 6 20634110 intron variant C/T snv 0.19 1
rs9460550 1.000 0.080 6 20719330 intron variant G/A snv 0.30 1
rs9460546 1.000 0.080 6 20663401 intron variant T/G snv 0.40 1
rs9460545 1.000 0.080 6 20661319 intron variant T/A;C snv 1
rs9460544 1.000 0.080 6 20661298 intron variant G/A;T snv 1
rs9460540 1.000 0.080 6 20648531 intron variant A/G snv 0.35 1
rs9460538 1.000 0.080 6 20640306 intron variant G/A snv 0.70 1
rs9368226 1.000 0.080 6 20722826 intron variant T/C snv 0.29 1
rs9368224 1.000 0.080 6 20719001 intron variant T/A snv 0.30 1
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs9368219 1.000 0.080 6 20674460 intron variant C/T snv 0.19 3
rs9368216 1.000 0.080 6 20654879 intron variant A/C;G snv 1
rs9358358 1.000 0.080 6 20719162 intron variant A/C snv 0.19 1
rs9358357 1.000 0.080 6 20718914 intron variant A/G snv 0.30 1
rs9358356 1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs9358355 1.000 0.080 6 20654666 intron variant T/C snv 0.27 1
rs9356748 1.000 0.080 6 20724866 intron variant T/A snv 0.14 1
rs9356747 1.000 0.080 6 20724776 intron variant T/A snv 0.35 1
rs9356746 1.000 0.080 6 20720048 intron variant T/C snv 0.15 1