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 2012 2012
dbSNP: rs2268575
rs2268575
GCK ; LOC105375258
2 7 44149675 intron variant T/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs2908289
rs2908289
GCK ; LOC105375257
3 1.000 0.080 7 44184343 intron variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2971671
rs2971671
GCK ; LOC105375257
2 7 44171738 intron variant T/C snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6975024
rs6975024
GCK
4 7 44192287 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012