Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs3025684
CREBBP
1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 2
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs774847933
COMT ; MIR4761
0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 5