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: rs1036483919
rs1036483919
GCK
4 0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 0.020 1.000 2 2014 2016
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.020 1.000 2 2010 2016
dbSNP: rs104894014
rs104894014
GCK
3 0.925 0.080 7 44145167 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs1174670182
rs1174670182
GCK
3 0.925 0.080 7 44145616 synonymous variant A/T snv 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1444739794
rs1444739794
GCK
3 0.925 0.080 7 44153324 missense variant A/G snv 4.0E-06 0.010 < 0.001 1 1998 1998
dbSNP: rs193929373
rs193929373
GCK ; LOC105375258
4 0.882 0.120 7 44147723 missense variant C/T snv 0.010 1.000 1 2005 2005
dbSNP: rs556436603
rs556436603
GCK ; LOC105375258
3 0.925 0.080 7 44147690 missense variant G/A snv 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs749877032
rs749877032
GCK
3 0.925 0.080 7 44145551 missense variant T/C snv 4.2E-06 0.010 1.000 1 2016 2016
dbSNP: rs867232360
rs867232360
GCK
3 1.000 0.040 7 44145552 missense variant C/T snv 0.010 1.000 1 2007 2007