Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs2682826
NOS1
0.807 0.280 12 117215033 3 prime UTR variant G/A snv 0.25 11
rs3766871
RYR2
0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs702764
OPRK1
0.925 0.120 8 53229597 synonymous variant T/C;G snv 0.17; 8.0E-06 4
rs179991
ATXN1
6 16325331 intron variant C/T snv 0.66 1