GCKR, glucokinase regulator, 2646

N. diseases: 136; N. variants: 23
Disease: Serum albumin measurement ×
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: rs1260326
rs1260326 		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 5 2010 2018
dbSNP: rs780092
rs780092 		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 2 2011 2012
dbSNP: rs3817588
rs3817588 		0.882 0.160 2 27508345 intron variant T/C snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6547692
rs6547692 		1.000 0.080 2 27512105 intron variant G/A snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs780093
rs780093 		0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs780094
rs780094 		0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs780095
rs780095 		2 27518238 intron variant A/G snv 0.60
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs780096
rs780096 		2 27518205 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs814295
rs814295 		0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012