Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34516333
ZFHX3
16 73114768 intron variant G/T snv 0.17 1
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs202085145
SUOX
1.000 0.080 12 56002720 missense variant G/T snv 1.0E-03 5.6E-04 6
rs4951043
SOX13
1 204105737 intron variant C/T snv 0.51 1
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs2020936
SLC6A4
0.776 0.160 17 30223796 intron variant G/A;C snv 10
rs7194256
SLC6A2
0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs301430
SLC1A1 ; SPATA6L
0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs6462203
SDK1
7 3636370 intron variant C/A;T snv 1
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs757281
RAPGEF3
1.000 0.040 12 47748635 non coding transcript exon variant C/A;G;T snv 2
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs6030245
PTPRT
20 42441919 intron variant T/C snv 0.30 1