Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12 2
rs10159477
HK1
10 69340132 intron variant G/A snv 0.14 1