Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1260326
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 4 2010 2018
dbSNP: rs780092
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2011 2012