Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2245368 7 76978826 non coding transcript exon variant C/T snv 0.80 3
rs2430307 7 76980627 non coding transcript exon variant T/C snv 0.79 2
rs17149254 7 77005146 intron variant T/A;C snv 1
rs6951489 7 77010522 intron variant A/G snv 0.78 1
rs6954694 7 77002781 intron variant G/A;C snv 1