Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs466448
APP
0.925 0.040 21 26171790 intron variant A/C;G snv 4
rs2104425
LOC105375050
0.925 0.040 6 40277470 upstream gene variant T/C snv 0.91 4
rs3842803
PTGS1
0.925 0.040 9 122392256 synonymous variant T/C snv 2.4E-02 8.2E-02 4
rs6432860
SCN1A ; SCN1A-AS1
0.925 0.080 2 166041354 synonymous variant A/G;T snv 0.73; 4.0E-06 4
rs1514280
ACE2
1.000 X 15568325 intron variant A/G snv 3
rs10809907
MPDZ
1.000 9 13134433 non coding transcript exon variant C/G;T snv 3