Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs208294
P2RX7 ; LOC105370032
0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs7958311
P2RX7 ; LOC105370032
0.851 0.160 12 121167552 missense variant G/A;C snv 0.25; 4.0E-06 5
rs1718119
LOC105370032 ; P2RX7
0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs201059543
P2RX7 ; LOC105370032
12 121184366 missense variant C/G;T snv 4.0E-06; 3.6E-05 2
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs1057518927
OAT
0.925 0.080 10 124402952 missense variant T/C snv 4
rs73633565 X 13459192 intergenic variant A/G snv 0.14 1
rs1554781700
COL5A1
0.851 0.240 9 134701287 missense variant G/T snv 12
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs6827096
EDNRA
4 147514294 intron variant C/T snv 0.30 1
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs12654778
ADRB2
5 148826178 5 prime UTR variant G/A snv 0.34 1
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs4512126
ABLIM3
5 149166179 intron variant T/A;C snv 1
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs28935468
MECP2
0.732 0.240 X 154030912 missense variant G/A snv 17
rs61751364
MECP2
0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 4
rs61748421
MECP2
0.807 0.200 X 154031326 stop gained G/A;T snv 9
rs77114424
OPRM1
6 154039497 missense variant G/A snv 2
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs200207721
OPRM1
6 154039743 missense variant A/G snv 1.2E-05 1.4E-05 2
rs563649
OPRM1
1.000 0.040 6 154086832 5 prime UTR variant C/T snv 9.8E-02 2
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
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