Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11596587
rs11596587
HK1
1 1.000 10 69354232 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018