Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3003609
DNM1
1.000 0.080 9 128222476 synonymous variant C/T snv 0.54 0.42 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs5320
DBH
0.882 0.120 9 133642351 missense variant G/A snv 6.7E-02 8.5E-02 3
rs1541333
DBH
1.000 0.080 9 133646263 intron variant C/G snv 0.52 1
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs4424567
FRMD4A
1.000 0.080 10 13759269 3 prime UTR variant A/G snv 0.25 1
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs557748
OPRM1
1.000 0.080 6 154043167 intron variant G/A snv 0.19 1
rs774507706
OPRM1
1.000 0.080 6 154091093 missense variant A/G snv 4.0E-06 1
rs4845652
LOC107985206
1.000 0.080 1 154565729 non coding transcript exon variant C/A;T snv 1
rs2072660
CHRNB2
1.000 0.080 1 154576245 3 prime UTR variant T/C;G snv 1
rs4425326
NPY2R
0.925 0.080 4 155186084 intron variant C/T snv 0.47 2
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
rs10798059
PLA2G4A
0.925 0.080 1 186830478 intron variant G/A snv 0.40 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs12466358
CHRND
1.000 0.080 2 232532815 intron variant T/G snv 0.22 1
rs1162419578
APP
0.925 0.160 21 25975126 missense variant G/A snv 4.0E-06 2
rs3735757
CHRNA2
1.000 0.080 8 27464080 intron variant G/A;C;T snv 1