Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1434282 1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs7529925 1 199038079 intron variant C/T snv 0.77 3
rs1036332 1 199043349 intron variant A/C snv 0.70 2
rs781255974 1 199025568 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs6427756 1 199031598 intron variant A/G snv 0.71 1
rs115858175 1.000 0.040 1 199032122 intron variant C/A;G snv 1