GCG, glucagon, 2641

N. diseases: 441; N. variants: 10
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1037733674
rs1037733674
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2001 2001
dbSNP: rs183433761
rs183433761
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015