Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs4659682
LGALS8
1 236518948 intron variant A/G snv 0.62 1
rs6736017
PSMD1 ; HTR2B
2 231108702 missense variant T/C snv 6.3E-03 2.5E-02 4
rs79874540
PSMD1 ; HTR2B
0.925 0.080 2 231123707 stop gained G/A snv 1.5E-03 1.2E-03 4
rs886041097
NAA15
0.882 0.160 4 139386152 stop gained C/G snv 9
rs2044081
GABRB1
1.000 0.080 4 47216323 intron variant C/T snv 0.14 2
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs10078866
DRD1
1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 2
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs1554210073
PHIP
0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs1131691771
PHIP ; IRAK1BP1
0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs1562150844
PHIP
0.790 0.280 6 78982908 frameshift variant CTTT/- delins 14
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs806379
CNR1
1.000 0.040 6 88151548 intron variant A/C;T snv 2