Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3088050 5 177299634 3 prime UTR variant G/A snv 0.18 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4640244 17 21380911 intron variant A/G snv 0.33 1
rs4686340 3 9303534 intron variant A/C snv 0.80 1
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs55747707 7 73623036 intron variant G/A snv 0.16 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs6486060 11 9003083 intron variant G/A snv 0.55 1
rs6701231 1 118953038 intron variant C/A;G snv 1
rs6861681 5 173935455 intron variant G/A snv 0.22 1
rs6931262 6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs6942652 7 121249218 intron variant G/C;T snv 1
rs7246865 19 17108295 intron variant G/A snv 0.36 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7745274 6 127188012 intron variant G/A snv 0.56 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9491696 6 127131494 intron variant C/G snv 0.45 1
rs9647379 3 172067378 intron variant G/C snv 0.32 1
rs984222 1 118961220 intron variant C/A;G snv 1
rs987763 6 126960402 intron variant C/A;T snv 1
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20