Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs147484110
CSTB
0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs1267306614
DRD3
1.000 0.080 3 114171850 missense variant C/G snv 1
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs2293054
NOS1
0.925 0.080 12 117263909 synonymous variant A/G;T snv 0.69; 4.0E-06 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs4911871
MIR1911 ; LOC105373313 ; HTR2C
1.000 0.080 X 114762580 intron variant A/G snv 0.15 1
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs1563945076
APTX
0.925 0.160 9 32974556 frameshift variant A/- del 4
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7