Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1344674 3 141406344 intron variant A/G snv 0.55 2
rs1991431 3 141414608 intron variant G/A snv 0.50 2
rs2871960 3 141402972 5 prime UTR variant A/C snv 0.55 2
rs6763931 0.925 0.080 3 141383991 intron variant G/A snv 0.54 2
rs10513137 3 141424588 intron variant G/A;C snv 1
rs6440003 3 141375367 intron variant G/A snv 0.54 1
rs6764769 3 141381438 5 prime UTR variant A/G snv 0.54 1
rs724016 1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 1
rs9825379 3 141418193 intron variant G/A snv 0.13 1