Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10005540 4 173660916 downstream gene variant C/G;T snv 1
rs10041818 5 148691691 intergenic variant C/T snv 0.35 1
rs10088136 8 85482363 downstream gene variant T/A snv 0.64 1
rs10089933 8 48478923 intergenic variant T/C snv 0.32 1
rs10136987 14 93842954 intergenic variant G/A snv 0.89 1
rs10201883 2 177606679 intron variant T/C snv 0.82 1
rs10214145 5 27636685 intergenic variant T/A;G snv 1
rs1035101 2 59563217 intron variant C/T snv 0.60 1
rs1041733 21 34311960 intron variant T/A snv 0.49 1
rs1074993 12 12281304 regulatory region variant A/G snv 0.75 1
rs10779447 1 221587993 intergenic variant A/G snv 0.35 1
rs1080278 2 209410985 intergenic variant G/A snv 0.22 1
rs10850533 12 109645636 regulatory region variant G/C snv 0.67 1
rs10914269 1 31096384 upstream gene variant G/T snv 0.70 1
rs10917165 1 22175135 intergenic variant T/C snv 0.34 1
rs11031736 11 32350208 intergenic variant G/A;C snv 1
rs11049733 12 28600467 intergenic variant C/T snv 0.48 1
rs11077539 17 70980861 intergenic variant T/A;C;G snv 1
rs11082082 18 22684222 intergenic variant G/A snv 0.38 1
rs11086748 20 39379415 intergenic variant T/A;G snv 0.46 1
rs11097881 4 105127406 intergenic variant G/A snv 0.27 1
rs111962736 1 118739138 regulatory region variant A/G snv 4.0E-02 1
rs114962105 2 118903367 intergenic variant A/G snv 4.5E-03 1
rs115979533 1 21939837 upstream gene variant C/G snv 1.3E-02 1
rs11653958 17 64690612 intergenic variant G/A snv 0.81 1