Disease: Diabetes mellitus autosomal dominant type II (disorder)
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148311934
LOC105375258 ; GCK
0.827 0.080 7 44149763 missense variant C/T snv 8.0E-06 1.4E-05 5
rs587780345
LOC105375258 ; GCK
0.851 0.080 7 44150004 missense variant C/T snv 5
rs1360415315
LOC105375258 ; GCK
0.851 0.080 7 44149772 missense variant C/G;T snv 4.0E-06 4
rs193922283
GCK
0.851 0.080 7 44145176 missense variant G/A snv 4
rs769268803
GCK ; LOC105375258
0.851 0.080 7 44147747 missense variant C/G;T snv 4.0E-06 4