Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs146539065
SEPSECS
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 17
rs139455627
TSPEAR
0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs147484110
CSTB
0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs74315442
CSTB
0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs864309483
ADCY5
0.851 0.080 3 123352464 missense variant G/A snv 9
rs113994152
TSEN54
0.790 0.160 17 75522000 missense variant G/T snv 9.0E-04 9.0E-04 9
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1563945076
APTX
0.925 0.160 9 32974556 frameshift variant A/- del 4
rs1064794533
GNAO1
0.882 0.080 16 56336846 missense variant G/A snv 4
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 3
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 3
rs752513525
NDUFA13
0.882 0.120 19 19526257 missense variant G/A;T snv 2.4E-05 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs387907128
LOC112268170 ; PRRT2
0.925 0.080 16 29813850 missense variant C/T snv 4.0E-06 7.0E-06 1
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 1
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 1