Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78352137 14 100454079 intron variant T/C snv 7.7E-02 2
rs10144321 14 100416068 intron variant A/G snv 0.24 1
rs12894936 14 100380654 intron variant T/C snv 0.55 1