Gene: GCG ×
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: rs1303328174
rs1303328174
GCG ; LOC101929532
1 1.000 0.120 2 162144042 missense variant G/T snv 0.010 1.000 1 2002 2002
dbSNP: rs375960284
rs375960284
GCG ; LOC101929532
1 1.000 0.120 2 162145570 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs5650
rs5650
GCG ; LOC101929532
1 1.000 0.120 2 162145588 missense variant G/A snv 0.010 1.000 1 2002 2002