Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3760396
CCL2
0.732 0.280 17 34254422 upstream gene variant G/C snv 0.15 13
rs3917887
CCL2
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33 8
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs2857656
CCL2
0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs13900
CCL2
0.925 0.120 17 34256892 3 prime UTR variant C/T snv 0.28 2
rs746076530
CCL2
1.000 0.080 17 34256238 synonymous variant A/G snv 1.6E-05 7.0E-06 1
rs760761240
CCL2
1.000 0.080 17 34256290 missense variant G/A;C snv 6.0E-05 1
rs2857657
CCL2
1.000 0.040 17 34256113 non coding transcript exon variant G/C snv 0.86 1