Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs61888800
BDNF
0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 5
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs10447760 0.851 0.040 7 114083210 upstream gene variant C/T snv 0.17 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs7294919 0.851 0.080 12 116889787 regulatory region variant T/C snv 0.19 4
rs4238989
AANAT
0.851 0.120 17 76467306 intron variant C/G snv 0.45 4
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325
BCL9
0.851 0.040 1 147605490 intron variant G/A snv 0.19 4