Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554700718
HNRNPK
0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs796052505
GABRG2
0.724 0.440 5 162095551 missense variant G/A;C snv 57
rs1554333853
CDK13
0.689 0.320 7 40046006 missense variant A/G snv 54
rs199469465
SRCAP
0.672 0.560 16 30737343 stop gained C/A;T snv 50
rs1057524820
SCN8A
0.776 0.280 12 51765746 missense variant G/A;T snv 33
rs1555528356
ANKRD11
0.790 0.360 16 89282836 stop gained G/A snv 13
rs758946412
PCDH19
0.790 0.240 X 100407507 frameshift variant G/-;GG delins 12