Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13300663 9 4814948 intron variant G/A;C snv 3
rs10974808 9 4840380 intron variant A/G snv 9.0E-02 2
rs423955 9 4792339 upstream gene variant C/A;G;T snv 0.56 1
rs457287 9 4834394 intron variant A/G;T snv 1