Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518946
GJB1
0.882 0.080 X 71223816 missense variant G/T snv 8
rs222747
TRPV1
0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs2653349
HCRTR2
0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06 5
rs751416416
OPRK1
0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5
rs7958311
P2RX7 ; LOC105370032
0.851 0.160 12 121167552 missense variant G/A;C snv 0.25; 4.0E-06 5
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs1057518927
OAT
0.925 0.080 10 124402952 missense variant T/C snv 4
rs61751364
MECP2
0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 4
rs80338761
SEPTIN9
0.882 0.080 17 77402298 missense variant C/T snv 4
rs8904
NFKBIA
0.925 0.120 14 35402011 3 prime UTR variant G/A;C;T snv 0.39; 4.0E-06 4
rs1051660
OPRK1
1.000 0.080 8 53251002 synonymous variant C/A;T snv 0.11 3
rs324419
FAAH
0.925 0.120 1 46406314 stop gained T/A;C snv 0.87 3
rs6334
NTRK1
1.000 0.080 1 156876441 missense variant G/A;C;T snv 0.22; 4.0E-06 3
rs104894379
TBX5
1.000 0.120 12 114398675 stop gained G/A;C;T snv 2
rs1288779666
NDUFA6-DT ; CYP2D6 ; LOC112268294
1.000 0.120 22 42128944 missense variant C/G snv 2
rs201059543
P2RX7 ; LOC105370032
12 121184366 missense variant C/G;T snv 4.0E-06; 3.6E-05 2
rs33985936
SCN11A
3 38894643 missense variant C/A;T snv 8.0E-06; 0.22 2
rs376128467
SCN11A
3 38894920 missense variant A/G;T snv 4.0E-06 2
rs3766246
FAAH
1 46399999 intron variant A/C;G snv 2
rs5993882
COMT
22 19950010 intron variant T/C;G snv 2
rs748653984
NTRK1
1.000 0.080 1 156868159 missense variant T/A;C snv 4.0E-06; 4.0E-06 2