Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs373611092
MIR4761 ; COMT
0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05 5
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95 3
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 3
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs200207721
OPRM1
6 154039743 missense variant A/G snv 1.2E-05 1.4E-05 2
rs6473799
OPRK1
8 53240563 intron variant A/G snv 0.39 2
rs749415280
UGT2B7
1.000 0.120 4 69096638 missense variant A/G snv 2
rs11898284
SCN1A-AS1 ; SCN9A
2 166325017 intron variant A/G snv 0.15 1
rs1571138 1 46429969 upstream gene variant A/G snv 0.73 1
rs7335912 13 95015426 upstream gene variant A/G snv 0.16 1
rs73633565 X 13459192 intergenic variant A/G snv 0.14 1
rs7718461
CRHBP
5 76962223 intron variant A/G snv 0.51 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
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
rs376128467
SCN11A
3 38894920 missense variant A/G;T snv 4.0E-06 2
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs7016778
OPRK1
8 53237545 intron variant A/T snv 0.17 3
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48