Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1346408 3 141353447 intron variant C/T snv 0.55 1
rs6440001 3 141367130 3 prime UTR variant T/C snv 0.52 1
rs6784404 3 141354833 intron variant G/A snv 0.54 1
rs7613516 3 141360467 intron variant T/G snv 0.56 1
rs9866391 1.000 0.040 3 141357242 intron variant T/C snv 0.41 1