Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 2
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs886037776
EHMT1
0.925 0.280 9 137817477 stop gained G/A snv 2
rs878853161
SLC2A1
0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs4534
GML ; CYP11B1
0.925 0.240 8 142879686 missense variant C/T snv 8.4E-02 4.1E-02 1
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 1
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 1
rs587777457
MAOA
0.925 0.200 X 43731695 missense variant G/T snv 1
rs769236847
CZ1P-ASNS ; ASNS
0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 1
rs878853147
NLGN3
0.925 0.200 X 71169399 missense variant C/T snv 1
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 11
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7