Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs10879357
TPH2
1.000 0.040 12 72020783 intron variant A/G snv 0.59 1
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs4795942
TMEM132E
1.000 0.040 17 34584149 intron variant C/T snv 0.72 1
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
rs7309727
TMEM132D
1.000 0.040 12 129470814 intron variant T/C snv 0.75 1
rs8076112
TLCD2
1.000 0.040 17 1708905 intron variant A/C;G snv 0.15 1
rs7788
SNAPC2
1.000 0.040 19 7923232 3 prime UTR variant T/C snv 0.28 1
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs4583306
SLC6A4
1.000 0.040 17 30211697 intron variant A/G snv 0.37 1
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs1805067
SLC6A2
0.925 0.080 16 55698511 missense variant G/A snv 2.8E-05 2.1E-05 2
rs10216809
SGCZ
0.925 0.080 8 14507414 intron variant C/G;T snv 2
rs3816995
SDK2
1.000 0.040 17 73339121 intron variant G/A snv 0.40 1
rs11805657
RGS7
1.000 0.040 1 240955726 intron variant T/C snv 0.87 1
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16