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
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
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
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
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
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs9836592
CHDH
0.925 0.120 3 53821056 intron variant C/T snv 0.74 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs12701020
CRHR2
0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs113507694
DPPA3
1.000 0.040 12 7714013 intron variant A/G snv 3.2E-02 1
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2