Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs864309483
ADCY5
0.851 0.080 3 123352464 missense variant G/A snv 9
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs1064794533
GNAO1
0.882 0.080 16 56336846 missense variant G/A snv 4
rs1563945076
APTX
0.925 0.160 9 32974556 frameshift variant A/- del 4
rs393795
SLC6A3
0.851 0.160 5 1428399 intron variant G/T snv 0.28 4
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs1267306614
DRD3
1.000 0.080 3 114171850 missense variant C/G snv 1
rs1345423
GRIN2A
1.000 0.080 16 10154207 intron variant G/A;C;T snv 1
rs4911871
MIR1911 ; LOC105373313 ; HTR2C
1.000 0.080 X 114762580 intron variant A/G snv 0.15 1