Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 4
rs387906639
HARS1 ; DND1
0.925 0.120 5 140674776 missense variant T/G snv 2.0E-05 9.1E-05 4
rs2396753
FOXP2
0.925 0.160 7 114508276 intron variant C/A;G snv 3
rs3751082
ALDH3B1
0.925 0.160 11 68027885 synonymous variant G/A snv 0.21 0.19 2
rs474559 1.000 0.120 9 32614094 regulatory region variant G/A snv 1.1E-02 1
rs1426891
LINC02248 ; LOC105370740
1.000 0.120 15 26472746 intron variant G/A snv 0.29 1
rs2912602
LINC02248 ; LOC105370740
1.000 0.120 15 26474092 intron variant G/A snv 0.16 1
rs2912600
LOC105370740 ; LINC02248
1.000 0.120 15 26475396 intron variant A/G snv 0.28 1