Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 5
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 4
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs111940429
LINC01789
0.925 0.080 2 107366232 intron variant C/A;T snv 2
rs145763646
SLC25A26
0.925 0.080 3 66173478 intron variant G/A snv 0.13 2
rs17110563
TPH2
0.827 0.080 12 71972526 missense variant C/T snv 1.2E-03 1.1E-03 2
rs17138230
TENM4
0.925 0.080 11 79364808 intron variant A/T snv 0.16 2
rs17810023
BCKDHB
0.925 0.080 6 80443056 non coding transcript exon variant C/T snv 1.7E-02 2
rs182107583
MMADHC-DT
0.925 0.080 2 149675023 intron variant A/C snv 4.2E-03 2
rs1950038 0.925 0.080 2 183579642 regulatory region variant T/C snv 0.71 2
rs6006893
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44858015 intron variant C/T snv 0.15 2
rs726170
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44855931 intron variant C/T snv 0.15 2
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs7337127 0.925 0.080 13 104623579 intergenic variant C/A;T snv 2
rs76087671
LOC105372577
0.925 0.080 20 24330541 intergenic variant C/A;G;T snv 2
rs7904579
CUBN
0.925 0.080 10 17089754 intron variant G/A;C snv 2
rs7932890
TENM4
0.925 0.080 11 79357349 intron variant A/G snv 0.19 2
rs9829032
CADM2
0.925 0.080 3 85634450 intron variant A/G snv 0.41 2
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 1
rs12456492
RIT2
0.882 0.080 18 43093415 intron variant A/G snv 0.33 1
rs12493050
LAMP3
0.925 0.080 3 183147285 intron variant G/A;C snv 1