Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs2238732
PRODH
22 18927834 intron variant C/G;T snv 7
rs17450273 12 102967601 intergenic variant C/A;T snv 4
rs17450122
ASCL1
12 102960616 upstream gene variant A/C;G;T snv 2
rs6807064
ATP2B2
3 10494087 intron variant C/T snv 0.35 2
rs1718302
PAH
12 102878908 intron variant G/A snv 0.89 2
rs78985461
PAH
12 102901858 intron variant G/A snv 0.14 2