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 0.830 0.750 4 2008 2013
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: rs1360415315
rs1360415315
GCK ; LOC105375258
4 0.851 0.080 7 44149772 missense variant C/G;T snv 4.0E-06 0.700 0
dbSNP: rs148311934
rs148311934
GCK ; LOC105375258
5 0.827 0.080 7 44149763 missense variant C/T snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs193922283
rs193922283
GCK
4 0.851 0.080 7 44145176 missense variant G/A snv 0.700 0
dbSNP: rs587780345
rs587780345
GCK ; LOC105375258
5 0.851 0.080 7 44150004 missense variant C/T snv 0.700 0
dbSNP: rs769268803
rs769268803
GCK ; LOC105375258
4 0.851 0.080 7 44147747 missense variant C/G;T snv 4.0E-06 0.700 0
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 2012 2014
dbSNP: rs587780346
rs587780346
GCK ; LOC105375258
3 0.925 0.080 7 44149823 missense variant T/G snv 0.010 1.000 1 2012 2012
dbSNP: rs730497
rs730497
GCK ; LOC105375257
4 0.882 0.160 7 44184122 intron variant G/A snv 0.17 0.010 1.000 1 2010 2010