Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs1701137
VPS53
0.882 0.080 17 572682 intron variant C/T snv 0.50 3
rs57083693
UTP20
1.000 0.080 12 101348402 intron variant T/C snv 0.23 3
rs3736802
TRPC4AP
1.000 0.080 20 35016239 intron variant T/C snv 0.53 3
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs11623335
TMEM260
1.000 0.080 14 56566358 intron variant G/A snv 0.85 1
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs10496768
THSD7B
1.000 0.080 2 137322384 intron variant G/A snv 9.5E-02 1
rs1869324
THSD7B
1.000 0.080 2 137469872 intron variant G/A snv 7.9E-02 1
rs6356
TH
0.827 0.240 11 2169721 missense variant C/T snv 0.43 0.32 5
rs3771856
TACR1 ; LOC105374811 ; LOC105374812
0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57 3
rs6715729
TACR1 ; LOC105374811
1.000 0.080 2 75198602 synonymous variant A/G snv 0.48 0.58 1
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs735668
TACR1
1.000 0.080 2 75135918 intron variant A/C;G snv 1
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs11583322
STK40
1.000 0.080 1 36356711 intron variant T/C snv 0.30 1
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs2567608
SSTR4
0.925 0.080 20 23036445 missense variant T/A;C snv 2.8E-05; 0.49 2
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs248793
SRD5A1 ; NSUN2
1.000 0.080 5 6633666 synonymous variant C/G snv 0.55 0.58 1
rs12489456
SLC6A6
1.000 0.080 3 14459666 intron variant G/A;T snv 1
rs3773165
SLC6A6
1.000 0.080 3 14482762 intron variant G/A snv 0.20 1
rs1443547
SLC6A5
1.000 0.080 11 20601429 missense variant G/A snv 0.37 0.38 1