Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs1326656542
LIG4
0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs1245554802
CAMK1 ; OGG1
0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs754635
CCK
1.000 0.040 3 42263639 splice region variant C/G;T snv 0.84; 5.6E-06 3
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs11946004
NPY5R
0.925 0.040 4 163351551 synonymous variant G/A;T snv 0.10; 4.0E-06 2
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs10875995
ASIC1
1.000 0.040 12 50068355 intron variant T/A;C snv 1
rs13356494 1.000 0.040 5 135991866 regulatory region variant C/G;T snv 1
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs16938184
PRDM11
1.000 0.040 11 45179068 intron variant G/A;C snv 1
rs1819741 1.000 0.040 1 192815708 intron variant T/A;C snv 1
rs37790 1.000 0.040 5 53346682 intergenic variant C/G;T snv 1