Disease: Sleep disturbances
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs1555743003
ASXL3
0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs1557043622
SLC35A2
0.695 0.400 X 48909843 missense variant C/A snv 46
rs267606826
FOXG1
0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs1555462347
USP7
0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs1060499733
DHX30
0.851 0.120 3 47846757 missense variant A/G snv 11