Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4
rs10170218 1.000 0.040 2 187949717 intron variant A/C snv 0.25 1
rs3100127 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 1
rs406001 1.000 0.040 7 51938719 intergenic variant T/A;C snv 1
rs682457 1.000 0.040 11 88216364 intergenic variant T/C snv 0.14 1
rs717947 1.000 0.040 4 33652135 intron variant C/A;T snv 1
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs263232
ADCY8
1.000 0.040 8 130795923 intron variant C/A snv 6.7E-02 1
rs2267735
ADCYAP1R1
0.925 0.120 7 31095890 intron variant C/G snv 0.47 2
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs10852889
ALOX12 ; ALOX12-AS1
1.000 0.040 17 6997526 intron variant C/A;G;T snv 1
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs11599164
ANK3
1.000 0.040 10 60072226 missense variant G/T snv 7.2E-02 7.3E-02 1
rs17208576
ANK3
1.000 0.040 10 60074815 synonymous variant G/A snv 7.2E-02 7.3E-02 1
rs28932171
ANK3
1.000 0.040 10 60071532 missense variant T/C snv 7.2E-02 7.3E-02 1
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs159572
ANKRD55
1.000 0.040 5 56211219 intron variant A/C snv 0.37 1
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3852144
C5orf67
1.000 0.040 5 56566769 intron variant A/G snv 0.37 1
rs1990322
CACNA1C
1.000 0.040 12 2651804 intron variant G/A snv 0.69 0.57 1
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23