Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs3917887
CCL2
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33 8
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs11003125
MBL2
0.790 0.480 10 52772254 upstream gene variant G/C snv 0.31 7
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs140920120
BMP4
0.925 0.080 14 53952099 missense variant C/A;G snv 2.8E-04 2