Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779027563
CNTNAP1
0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs1060499548
ABL1
0.724 0.440 9 130872961 missense variant G/A snv 27
rs1555528356
ANKRD11
0.790 0.360 16 89282836 stop gained G/A snv 13
rs1555043939
KMT2A
0.851 0.240 11 118496323 frameshift variant -/G delins 9