Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 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
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs1655285
TSNAX-DISC1 ; TSNAX
1 231563728 intron variant G/C snv 9.5E-02 1
rs1959536
TRIM9
1.000 0.040 14 50980053 intron variant T/G snv 9.7E-02 2
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs17110747
TPH2
0.882 0.120 12 72032174 3 prime UTR variant G/A snv 0.12 4
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 3
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6081541
SLC24A3
1.000 0.040 20 19232246 intron variant A/G snv 0.20 2
rs1555910162
SHANK3
0.925 0.080 22 50721469 frameshift variant -/C delins 5
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2