Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs78089757 0.882 0.120 10 125424260 intergenic variant G/A snv 9.9E-03 3
rs11265269 1.000 0.080 1 159758337 upstream gene variant T/C snv 0.26 1
rs17135889
ABCA3
0.925 0.080 16 2337259 intron variant G/A snv 0.11 2
rs4351
ACE
0.925 0.160 17 63492371 intron variant G/A snv 0.50 3
rs371131106
ACE
0.925 0.120 17 63485346 missense variant A/G snv 8.4E-05 1.6E-04 2
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs35320474
ADORA2A ; SPECC1L-ADORA2A ; ADORA2A-AS1
1.000 0.080 22 24441941 3 prime UTR variant -/T delins 2
rs1010419
AGBL1
1.000 0.080 15 86992870 intron variant A/G snv 0.55 1
rs2701405
AGBL1
1.000 0.080 15 86996687 intron variant C/A snv 0.51 1
rs10152333
AGBL1-AS1 ; AGBL1
1.000 0.080 15 86311128 intron variant T/C snv 0.57 1
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
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
rs2284017
CACNG2
0.925 0.120 22 36700882 intron variant T/C snv 0.44 2
rs2284018
CACNG2
0.925 0.120 22 36701519 intron variant C/G;T snv 2
rs9836592
CHDH
0.925 0.120 3 53821056 intron variant C/T snv 0.74 2
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11