Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs2267716
CRHR2
0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs1470452230
PAEP
0.925 0.120 9 135561895 missense variant A/C snv 7.0E-06 2
rs10776934 1.000 0.080 9 135137855 regulatory region variant T/G snv 0.74 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs2854116
APOC3
0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs2854117
APOC3
0.851 0.200 11 116829426 upstream gene variant T/A;C snv 6
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs1293762
OAS2
1.000 0.080 12 112993031 intron variant T/G snv 0.67 1
rs11854484
SLC28A2 ; LOC101928414
0.925 0.120 15 45253280 missense variant C/T snv 0.47 0.45 2
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37