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
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs121912678
ACVR1
0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs8103142
IFNL3
0.882 0.120 19 39244466 missense variant T/C snv 0.29 0.40 4