Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs35134
ERAP1
5 96823820 intron variant A/G snv 0.65 1
rs943346
SORBS1
10 95494548 intron variant C/G;T snv 2
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7694531
UNC5C
4 95165950 3 prime UTR variant A/G snv 0.64 2
rs2011567
NDUFAF6
8 94959692 intron variant G/A;C snv 1
rs1361600
MIR12133 ; F3
0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs10786156
PLCE1
10 94254865 intron variant C/G snv 0.44 0.47 2
rs10882397
PLCE1
10 94132902 intron variant C/A snv 0.52 2
rs9658668
CHGA
14 92932724 missense variant C/T snv 3.9E-04 1.2E-03 1
rs740047
LOC105375397
7 92600848 downstream gene variant C/T snv 0.77 1
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs1314386070
DECR1
0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs2460448
DPEP1
16 89634473 intron variant G/A;C snv 1
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs532019808
NOX4
0.827 0.120 11 89451807 missense variant G/A;C snv 4.0E-06; 4.0E-06 8
rs6679817 1 88897581 intergenic variant C/T snv 0.25 1
rs10042590 5 88477501 intron variant G/A snv 5.8E-02 1
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs7698623
MEPE
4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 2