Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
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
rs17260539 1.000 0.040 9 12182545 intergenic variant G/A snv 6.6E-02 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
rs4145262 1.000 0.040 12 105659532 regulatory region variant C/A snv 4.8E-02 1
rs4448731 1.000 0.040 12 71935326 upstream gene variant T/C snv 0.40 1
rs685012 1.000 0.040 12 50052620 upstream gene variant C/T snv 0.66 1
rs7301616 1.000 0.040 12 60214608 intron variant C/T snv 0.96 1
rs9372078 1.000 0.040 6 150592825 intergenic variant T/A snv 0.73 1
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs10875995
ASIC1
1.000 0.040 12 50068355 intron variant T/A;C snv 1
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
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
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs887230
C17orf102
1.000 0.040 17 34577567 non coding transcript exon variant C/T snv 0.82 0.85 1
rs887231
C17orf102
1.000 0.040 17 34577461 non coding transcript exon variant G/A snv 0.73 1