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: rs10160596
rs10160596 		11 65583893 non coding transcript exon variant G/A snv 0.20
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs10160596
rs10160596 		11 65583893 non coding transcript exon variant G/A snv 0.20
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs10160596
rs10160596 		11 65583893 non coding transcript exon variant G/A snv 0.20
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11227229
rs11227229 		11 65586679 intron variant G/A snv 0.45
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs11227229
rs11227229 		11 65586679 intron variant G/A snv 0.45
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs11606601
rs11606601 		11 65586968 intron variant C/A;G snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs11606601
rs11606601 		11 65586968 intron variant C/A;G snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs3741380
rs3741380 		1.000 0.040 11 65581592 missense variant G/A snv 0.48 0.48
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3741380
rs3741380 		1.000 0.040 11 65581592 missense variant G/A snv 0.48 0.48
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs3741380
rs3741380 		1.000 0.040 11 65581592 missense variant G/A snv 0.48 0.48
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs4601790
rs4601790 		11 65586435 intron variant A/G snv 0.23
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2014 2014
dbSNP: rs4601790
rs4601790 		11 65586435 intron variant A/G snv 0.23
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2014 2014
dbSNP: rs4601790
rs4601790 		11 65586435 intron variant A/G snv 0.23
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2014 2014
dbSNP: rs4601790
rs4601790 		11 65586435 intron variant A/G snv 0.23
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs6591182
rs6591182 		0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.700 1.000 1 2010 2010
dbSNP: rs6591182
rs6591182 		0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2010 2010