Gene: GCK ×
Source: CURATED ×
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
4 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.830 0.750 1 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