Gene: GCK ×
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: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2971672
rs2971672
GCK
4 7 44166307 intron variant A/C snv 0.44 0.700 1.000 1 2013 2013