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: rs1037733674
rs1037733674
GCG ; LOC101929532
5 0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 0.040 0.500 4 1996 2002
dbSNP: rs183433761
rs183433761
GCG ; LOC101929532
5 0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 0.010 1.000 1 2015 2015