Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10744891
NOS1
1.000 0.040 12 117284536 intron variant G/T snv 0.41 1
rs1187327
NTRK2
1.000 0.040 9 84673625 intron variant T/C snv 0.50 1
rs1033962
PRTFDC1
1.000 0.040 10 24927877 intron variant C/T snv 0.33 1
rs6482463
PRTFDC1
1.000 0.040 10 24924199 intron variant G/A snv 0.33 1
rs4511180
PTPRVP
1.000 0.040 1 202180311 non coding transcript exon variant A/G snv 0.65 1
rs363276
SLC18A2
1.000 0.040 10 117274298 intron variant T/C;G snv 1
rs356195
SNCA
1.000 0.040 4 89762017 intron variant T/C snv 0.81 1
rs451275
SPRY4-AS1
1.000 0.040 5 142392033 intron variant C/T snv 1
rs7866350
TBC1D2
1.000 0.040 9 98221544 intron variant C/G;T snv 0.20 1
rs6812849
TLL1
1.000 0.040 4 165951384 intron variant C/A;T snv 1
rs7691872
TLL1
1.000 0.040 4 165944433 intron variant G/C;T snv 1
rs2108977
TPH1
1.000 0.040 11 18019049 3 prime UTR variant T/C snv 0.47 1
rs4576167
WWC1
1.000 0.040 5 168459692 intron variant G/C snv 0.31 1
rs2267735
ADCYAP1R1
0.925 0.120 7 31095890 intron variant C/G snv 0.47 2
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs562010289
LAMC2
0.925 0.120 1 183227583 missense variant G/A;C snv 1.7E-04 2
rs6470292
LOC105375743 ; LINC00964
1.000 0.040 8 124855801 intron variant A/G snv 0.17 2
rs683250
LOC107984425 ; DLG2
1.000 0.040 11 83565125 intron variant A/G;T snv 2
rs4775301
RORA
0.925 0.040 15 60834660 intron variant T/C;G snv 2
rs8024133
RORA
0.925 0.040 15 60838440 intron variant C/T snv 0.42 2
rs8041061
RORA
0.925 0.040 15 60832639 intron variant G/T snv 0.39 2
rs7208505
SKA2
1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 2
rs182455
STMN1 ; LOC105376885
0.925 0.120 1 25908492 upstream gene variant A/G;T snv 2