Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72520913
MMP3
11 102845217 upstream gene variant -/C;G ins 1
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs1277774683
DNM2
19 10830162 missense variant A/C snv 4.0E-06 2.1E-05 1
rs398655 13 33013514 upstream gene variant A/C snv 0.51 1
rs4660928 1 46420268 TF binding site variant A/C snv 0.63 1
rs3766246
FAAH
1 46399999 intron variant A/C;G snv 2
rs773030005
UGT2B7
1.000 0.040 4 69107204 synonymous variant A/C;G snv 4.0E-06; 6.8E-05 2
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs540825
OPRM1
6 154093311 missense variant A/C;T snv 2.8E-05; 0.81 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs781565158
PYROXD1
0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 22
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7