Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56163822
NR1H4
1.000 0.080 12 100493323 5 prime UTR variant G/T snv 4.7E-02 2.8E-02 2
rs35724
NR1H4
0.925 0.040 12 100561600 intron variant C/G snv 0.52 3
rs1921
ISG15
1 1014228 missense variant G/A;C snv 0.36 1
rs104894630
SCO1
0.882 0.120 17 10692805 missense variant G/A snv 4
rs587777220
SCO1
0.882 0.120 17 10692932 missense variant C/T snv 1.2E-05 7.0E-06 4
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs4849133 2 112923864 downstream gene variant C/A;T snv 2
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs75961395
CFTR
0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs1420111973
TLR4
1.000 0.080 9 117712527 synonymous variant T/C snv 7.0E-06 2
rs954917585
FGFR2
10 121479973 missense variant G/A snv 8.0E-06 1.4E-05 1
rs868564661
FGFR2
10 121487415 missense variant G/A snv 1
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs121434622
FMR1
1.000 0.080 X 147936534 missense variant T/A snv 2
rs1290547844
BRD4
19 15273041 missense variant C/T snv 4.0E-06 1