Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs17718444
FOXP1
1.000 0.120 3 71450250 intron variant C/T snv 0.27 1
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs62408225
BACH2
1.000 0.120 6 90246690 intron variant A/G snv 0.26 2
rs828618
DCBLD2
0.925 0.160 3 98822789 intron variant G/A snv 0.28 0.22 2