Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1806201
GRIN2B
0.776 0.200 12 13564574 synonymous variant G/A snv 0.32 0.24 8
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs371308207
C1D
0.882 0.080 2 68047303 missense variant C/A;T snv 4.1E-06; 4.1E-06 4
rs11731003
SORCS2
1.000 0.080 4 7388545 intron variant C/G;T snv 1