Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045411
HMGB1
0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs17616
CR2
1.000 0.080 1 207473578 missense variant G/A snv 0.26 0.30 1
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs7309123
LOC105369655 ; CLEC7A
0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs213950
CFTR-AS1 ; CFTR
0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140