Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs2619538
DTNBP1
0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 4
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs769404
GAD1
1.000 0.040 2 170822115 synonymous variant T/C snv 0.39 0.35 2
rs701492
GAD1
1.000 0.040 2 170845970 intron variant C/T snv 0.30 0.28 2
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs6081541
SLC24A3
1.000 0.040 20 19232246 intron variant A/G snv 0.20 2
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs6046396
RIN2
20 19871859 non coding transcript exon variant G/A snv 0.68 2
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs737864
TXNRD2 ; COMT
1.000 0.040 22 19942636 intron variant C/T snv 0.23 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27