Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs241509
ATP2B2
1.000 0.040 3 10345375 intron variant C/A;T snv 0.45 1
rs3774180
ATP2B2
1.000 0.040 3 10355304 intron variant T/C snv 0.37 1
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs7294536
AVPR1A
0.925 0.040 12 63154312 upstream gene variant T/C snv 0.26 2
rs3759292
AVPR1A
1.000 0.040 12 63153533 intron variant A/G snv 2.4E-02 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
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs1163276899
CACNA1D
1.000 0.040 3 53673125 missense variant G/A snv 2
rs201292141
CADM1
1.000 0.040 11 115217961 missense variant T/G snv 3.9E-04 9.8E-05 1
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs2241694
CAMK2A
1.000 0.040 5 150223045 missense variant A/G snv 0.92 0.94 1
rs25925
CAMK4
0.925 0.040 5 111484055 synonymous variant G/C snv 0.75 0.83 2
rs750257282
CARS1 ; CARS1-AS1
1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3
rs7632287
CAV3
1.000 0.040 3 8749760 intron variant G/A snv 0.32 2
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs1042778
CAV3 ; OXTR
0.925 0.040 3 8752859 3 prime UTR variant G/A;C;T snv 3
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs237902
CAV3 ; OXTR
0.925 0.040 3 8767498 synonymous variant G/A snv 0.29 0.31 3
rs237889
CAV3 ; OXTR
0.925 0.040 3 8760797 intron variant T/C snv 0.71 2
rs2268494
CAV3 ; OXTR
1.000 0.040 3 8760360 intron variant T/A snv 6.2E-02 1
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8