Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs1801690
APOH
0.925 0.120 17 66212167 missense variant C/G snv 4.8E-02 4.0E-02 6
rs4581
APOH
0.851 0.160 17 66214639 missense variant C/A;G snv 0.38; 4.0E-06; 4.0E-06 0.36 5
rs267607591
LMNA
0.882 0.200 1 156135274 missense variant G/A snv 4
rs104895461
NOD2
0.882 0.120 16 50710912 missense variant G/A;C snv 4
rs1369837875
PLA2G6
0.882 0.200 22 38128276 synonymous variant G/A snv 4
rs3765187
CD36
0.925 0.160 7 80656687 missense variant C/T snv 3
rs104895477
NOD2
0.925 0.120 16 50711058 stop gained G/A;T snv 3.6E-05 3
rs79154414 1.000 0.040 2 67897074 intergenic variant C/T snv 6.6E-04 2
rs2288493
LOC101928462 ; TSHR
1.000 0.040 14 81145262 3 prime UTR variant C/T snv 0.15 2
rs1469042326
RIMS2
1.000 0.120 8 103885482 missense variant G/A snv 4.0E-06 2
rs1801692
APOH
17 66226046 missense variant C/T snv 3.9E-02 3.4E-02 1
rs1316724604
PROS1
3 93884748 missense variant G/C snv 1
rs777417437
PRR4 ; PRH1-PRR4 ; PRH1
12 10882293 missense variant C/A;T snv 4.1E-06 1