Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906686
SCN2A
0.742 0.320 2 165310413 missense variant C/A;T snv 23
rs879253767
SCN2A
0.882 0.080 2 165313738 frameshift variant T/- delins 6
rs796053134
SCN2A
0.827 0.080 2 165374737 missense variant T/C snv 5
rs869312663
SCN2A
0.882 0.200 2 165381114 missense variant A/G snv 5
rs387906684
SCN2A
0.851 0.120 2 165367327 stop gained G/A;T snv 4
rs796053124
SCN2A
0.882 0.080 2 165354232 missense variant G/T snv 4
rs869312664
SCN2A
0.925 0.160 2 165386920 stop gained G/A;T snv 4
rs1060503101
SCN2A
0.925 0.080 2 165388782 missense variant C/T snv 3
rs387906683
SCN2A
0.882 0.040 2 165297053 stop gained C/T snv 3
rs796053162
SCN2A
0.882 0.080 2 165389123 missense variant G/A snv 3
rs1057519524
SCN2A
0.925 0.040 2 165386837 missense variant T/C snv 2
rs1057519526
SCN2A
0.925 0.040 2 165344679 missense variant C/T snv 2
rs1057519527
SCN2A
0.925 0.040 2 165374743 missense variant G/A snv 2
rs1057519528
SCN2A
0.925 0.040 2 165310376 missense variant G/A snv 2
rs1060503102
SCN2A
0.925 0.080 2 165388682 stop gained C/T snv 2
rs121917751
SCN2A
0.925 0.080 2 165344666 missense variant G/A snv 2
rs121917752
SCN2A
0.925 0.080 2 165309414 missense variant G/A snv 2
rs1553461662
SCN2A
0.925 0.080 2 165377611 frameshift variant -/T delins 2
rs1553462227
SCN2A
0.925 0.080 2 165381148 missense variant T/C snv 2
rs1553463516
SCN2A
0.925 0.080 2 165388930 frameshift variant C/- delins 2
rs1553567409
SCN2A
0.925 0.080 2 165308794 missense variant C/T snv 2
rs1553567473
SCN2A
0.925 0.040 2 165309193 missense variant A/G snv 2
rs1553567561
SCN2A
0.925 0.080 2 165309431 missense variant T/G snv 2
rs1553568927
SCN2A
0.925 0.080 2 165313919 frameshift variant -/A delins 2
rs1553569054
SCN2A
0.925 0.080 2 165314067 stop gained C/T snv 2