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: rs193922331
rs193922331
GCK ; LOC105375258
4 0.882 0.080 7 44147726 missense variant A/G snv 7.0E-06 0.700 0
dbSNP: rs587780343
rs587780343
GCK
1 7 44145638 missense variant C/A;T 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: rs587780346
rs587780346
GCK ; LOC105375258
3 0.925 0.080 7 44149823 missense variant T/G snv 0.700 0
dbSNP: rs587780347
rs587780347
GCK ; LOC105375258
1 7 44147807 missense variant C/T snv 0.700 0
dbSNP: rs1799884
rs1799884
GCK
6 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.050 1.000 5 2013 2017
dbSNP: rs1036483919
rs1036483919
GCK
4 0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs4607517
rs4607517
GCK
8 0.882 0.080 7 44196069 intron variant G/A;C snv 0.010 < 0.001 1 2012 2012