Disease: Child Development Disorders, Pervasive
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10791111 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 2
rs1080500 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 2
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs11223651 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 2
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2
rs114142645 1.000 0.040 6 31245806 regulatory region variant T/C snv 2
rs114276265 1.000 0.040 6 31219298 upstream gene variant C/T snv 2
rs114291394 1.000 0.040 6 31383745 upstream gene variant A/C snv 2
rs114508985 1.000 0.040 6 32932241 downstream gene variant C/G;T snv 2
rs114830752 1.000 0.040 6 32715035 upstream gene variant C/A snv 2
rs114867672 1.000 0.040 6 30964067 upstream gene variant T/C snv 2
rs114882497 1.000 0.040 6 32423415 intergenic variant T/C snv 2
rs114904464 1.000 0.040 6 31380300 upstream gene variant G/A snv 2
rs1150688 1.000 0.040 6 28195002 intergenic variant T/C snv 0.54 2
rs115136442 1.000 0.040 6 31086734 downstream gene variant C/A snv 2
rs115165987 1.000 0.040 6 32239404 intergenic variant G/A snv 2
rs115329265 1.000 0.040 6 28744470 intergenic variant A/G;T snv 2
rs115569272 1.000 0.040 6 32995105 intergenic variant G/A snv 2
rs115682897 1.000 0.040 6 32725517 intergenic variant G/A snv 2
rs115687605 1.000 0.040 6 30397852 regulatory region variant C/T snv 2
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs116047537 1.000 0.040 6 32413695 TF binding site variant T/C snv 2
rs116067082 1.000 0.040 6 31222761 upstream gene variant G/A snv 2
rs116137698 1.000 0.040 6 28699892 intergenic variant A/G snv 2
rs116182620 1.000 0.040 6 32511744 intergenic variant A/G snv 5.8E-02 2