Source: ALL
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: rs193929373
rs193929373
GCK ; LOC105375258
4 0.882 0.120 7 44147723 missense variant C/T snv 0.010 1.000 1 2005 2005