Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9631541 1.000 0.080 3 23498288 intron variant A/G snv 0.22 1
rs9552911 1.000 0.080 13 23290518 intron variant G/A snv 1.2E-02 1
rs9505118 1.000 0.080 6 7290204 intron variant A/G snv 0.37 1
rs9502570 1.000 0.080 6 7258384 downstream gene variant C/T snv 0.38 1
rs9494266 1.000 0.080 6 135530435 intron variant G/A snv 0.27 1
rs9472138 0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 5
rs9470794 0.925 0.080 6 38139068 intron variant T/C snv 0.12 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
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs944082 1.000 0.080 1 68177408 intron variant T/C snv 0.55 1
rs9369425 0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
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