Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs1401635
BDNF ; BDNF-AS
0.925 0.040 11 27672444 intron variant C/G snv 0.73 2
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 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
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3