rs10224002, PRKAG2

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.800 1.000 1 2009 2009
Glomerular Filtration Rate
CUI: C0017654
Disease: Glomerular Filtration Rate
1033 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 2 2018 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 2 2016 2017
Corpuscular Hemoglobin Concentration Mean
4389 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2018 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2017 2017
Hemoglobin, CTCAE
CUI: C2239101
Disease: Hemoglobin, CTCAE
26 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 1 2009 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019