Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4608502 2 227269439 intron variant T/A;C snv 3
rs11553764 12 104021466 5 prime UTR variant C/T snv 0.13 2
rs28687756 16 88295322 intron variant T/G snv 6.5E-04 2
rs3118515 9 134544468 intron variant G/A;C;T snv 2
rs56009602 11 130419717 intron variant C/A;T snv 2