Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555038111
KMT2A
0.701 0.480 11 118478153 stop gained T/G snv 37
rs370717845
HGSNAT
0.763 0.320 8 43161462 missense variant G/A snv 33
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs1085308046
PTEN
0.790 0.240 10 87933160 missense variant T/C;G snv 9