Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001159 9 36728588 intergenic variant C/T snv 0.56 1
rs10057473 5 143507813 intron variant G/A;C snv 1
rs1010278 8 57641227 intron variant A/C;T snv 1
rs10115200 9 81451095 intergenic variant T/C snv 7.4E-02 1
rs1011685 8 19973258 regulatory region variant C/T snv 8.7E-02 1
rs10149929 14 98246151 intergenic variant G/A snv 0.31 1
rs10159927 10 8292500 intergenic variant G/A;C snv 1
rs1017217 5 164176197 intron variant G/A snv 0.94 1
rs10180633 2 20945069 intergenic variant G/T snv 0.41 1
rs10183548 2 20945739 intergenic variant G/A snv 0.41 1
rs10184054 2 20981005 intergenic variant C/G snv 0.23 1
rs10201247 2 27752104 intergenic variant A/G;T snv 1
rs10209020 2 27758077 intergenic variant C/T snv 0.63 1
rs1023616 5 164177605 intron variant T/C snv 0.94 1
rs1023818 13 69152910 intergenic variant A/G;T snv 1
rs10266035 7 124121351 intron variant G/A snv 0.13 1
rs1031028 11 13077683 intron variant C/T snv 8.2E-02 1
rs1033271 7 9669774 intron variant A/C;T snv 1
rs1036966 8 125777656 intron variant C/T snv 4.8E-02 1
rs10448340 9 136425617 downstream gene variant T/A;G snv 1
rs10506923 12 85758817 intergenic variant C/T snv 0.70 1
rs10518933 15 57794266 intergenic variant T/A;C snv 1
rs10521009 5 33894659 upstream gene variant G/A snv 0.63 1
rs10738976 9 36736814 intergenic variant T/C snv 0.58 1
rs10741271 10 127467534 intergenic variant A/C snv 0.79 1