Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2835859
KCNJ6
0.925 0.200 21 37645860 intron variant T/C snv 0.16 3
rs3845446
CACNA1E
1 181797301 intron variant T/C snv 6.3E-02 3
rs7016778
OPRK1
8 53237545 intron variant A/T snv 0.17 3
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 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
rs13080116
SCN11A
3 38865732 intron variant T/C snv 0.23 2
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs13361160 1.000 0.040 5 10169711 downstream gene variant T/C snv 0.34 2
rs1972597 1.000 0.040 17 77598082 intron variant T/C snv 0.31 2
rs2562456
LINC00664
1.000 0.040 19 21483408 non coding transcript exon variant C/T snv 0.77 2
rs2817040
LOC285847 ; ARMC12
6 35737829 intron variant G/A snv 0.22 2
rs3750625
ADRA2A
10 111079843 3 prime UTR variant C/A snv 8.7E-02 2
rs3766246
FAAH
1 46399999 intron variant A/C;G snv 2
rs3862188 1.000 0.040 1 247702471 intron variant T/C snv 0.44 2
rs563649
OPRM1
1.000 0.040 6 154086832 5 prime UTR variant C/T snv 9.8E-02 2
rs5993882
COMT
22 19950010 intron variant T/C;G snv 2
rs6473799
OPRK1
8 53240563 intron variant A/G snv 0.39 2
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
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
rs7734804
LOC105377703
5 164919530 intron variant G/T snv 8.3E-02 2
rs806378
CNR1
1.000 0.040 6 88149832 intron variant C/T snv 0.21 2
rs943552 1 156885826 downstream gene variant C/T snv 9.7E-02 2