Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs356195
SNCA
1.000 0.040 4 89762017 intron variant T/C snv 0.81 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs386231
NOS1AP
0.882 0.080 1 162356033 intron variant C/T snv 0.68 4
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs2074621
MIR6795 ; NOTCH3
1.000 0.040 19 15179601 non coding transcript exon variant G/A snv 0.67 1
rs4511180
PTPRVP
1.000 0.040 1 202180311 non coding transcript exon variant A/G snv 0.65 1
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1990322
CACNA1C
1.000 0.040 12 2651804 intron variant G/A snv 0.69 0.57 1
rs2400207
LOC107986458 ; SH3RF2
1.000 0.040 5 146000534 intron variant A/G snv 0.56 1
rs4523957
SMG6 ; SRR
0.790 0.120 17 2305605 intron variant G/T snv 0.54 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs1187327
NTRK2
1.000 0.040 9 84673625 intron variant T/C snv 0.50 1
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2267735
ADCYAP1R1
0.925 0.120 7 31095890 intron variant C/G snv 0.47 2
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs2108977
TPH1
1.000 0.040 11 18019049 3 prime UTR variant T/C snv 0.47 1
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77