Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs749415280
UGT2B7
1.000 0.120 4 69096638 missense variant A/G snv 2
rs76060075
NDUFA6-DT ; CYP2D6 ; LOC112268294
1.000 0.120 22 42129185 missense variant C/G snv 2
rs77114424
OPRM1
6 154039497 missense variant G/A snv 2
rs773030005
UGT2B7
1.000 0.040 4 69107204 synonymous variant A/C;G snv 4.0E-06; 6.8E-05 2
rs1172682117
ERG
21 38403690 synonymous variant T/G snv 4.0E-06 1
rs11988795
TRPA1 ; MSC-AS1
8 72037366 intron variant C/G;T snv 1
rs1292843126
SPNS1
16 28975269 missense variant G/A;C snv 1.6E-05 1
rs12948783
RHBDF2
17 76503318 upstream gene variant G/A;C;T snv 1
rs1378978590
NGFR ; LOC100288866 ; MIR6165
17 49510504 stop gained C/T snv 1
rs17122021 11 118274971 regulatory region variant C/A;T snv 1
rs200192163
MSC-AS1 ; TRPA1
8 72036453 missense variant C/A;G snv 1.6E-05 1
rs2211843
KCNJ6
21 37811882 intron variant G/C;T snv 1
rs2383515 1 186683820 upstream gene variant G/A;T snv 1
rs3872309
NBPF1
1 16564838 missense variant C/T snv 1
rs4512126
ABLIM3
5 149166179 intron variant T/A;C snv 1
rs4584690
ABCC4
13 95027878 intron variant T/C;G snv 1
rs540825
OPRM1
6 154093311 missense variant A/C;T snv 2.8E-05; 0.81 1
rs677830
OPRM1
6 154107531 stop gained C/A;G;T snv 6.6E-06; 6.6E-06; 0.19 1
rs72520913
MMP3
11 102845217 upstream gene variant -/C;G ins 1
rs769854785
NTRK1
1 156871656 synonymous variant C/T snv 1
rs7824175
OPRK1
8 53231614 intron variant C/G;T snv 1
rs80026734
CYP3A5 ; ZSCAN25
7 99676132 missense variant C/T snv 1
rs879254102
SCN9A ; SCN1A-AS1
2 166277257 missense variant C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs778056858
NTRK1
1.000 0.080 1 156866944 missense variant T/C snv 8.0E-06 7.0E-06 2