Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 5
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 3
rs730497
GCK ; LOC105375257
0.882 0.160 7 44184122 intron variant G/A snv 0.17 3
rs587780346
LOC105375258 ; GCK
0.925 0.080 7 44149823 missense variant T/G snv 2