Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs753626670
AFP
4 73437179 synonymous variant C/T snv 8.0E-06 1