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: rs867232360
rs867232360
GCK
3 1.000 0.040 7 44145552 missense variant C/T snv 0.010 1.000 1 2007 2007