Gene: GCK ×
Source: GWASCAT ×
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: rs4607517
rs4607517
GCK
2 0.882 0.080 7 44196069 intron variant G/A;C snv 0.800 1.000 6 2009 2019
dbSNP: rs1799884
rs1799884
GCK
2 1.000 0.080 7 44189469 intron variant C/T snv 0.17 0.800 1.000 2 2011 2019
dbSNP: rs2268575
rs2268575
GCK ; LOC105375258
1 7 44149675 intron variant T/C snv 0.18 0.800 1.000 1 2012 2019
dbSNP: rs730497
rs730497
GCK ; LOC105375257
1 0.882 0.160 7 44184122 intron variant G/A snv 0.17 0.700 1.000 2 2015 2019
dbSNP: rs10259649
rs10259649
GCK ; LOC105375257
1 7 44180106 intron variant T/C snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs2908290
rs2908290
GCK ; LOC105375257
3 1.000 0.040 7 44176538 intron variant G/A snv 0.43 0.700 1.000 1 2019 2019