H4C1, H4 clustered histone 1, 8359

N. diseases: 121; N. variants: 4
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: rs9467664
rs9467664 		0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 3 2010 2013
dbSNP: rs9467664
rs9467664 		0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 3 2010 2013
dbSNP: rs2157050
rs2157050 		0.925 0.120 6 26020203 upstream gene variant C/T snv 0.38
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs2157050
rs2157050 		0.925 0.120 6 26020203 upstream gene variant C/T snv 0.38
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs2157050
rs2157050 		0.925 0.120 6 26020203 upstream gene variant C/T snv 0.38
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2157050
rs2157050 		0.925 0.120 6 26020203 upstream gene variant C/T snv 0.38
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs41266779
rs41266779 		6 26021644 upstream gene variant C/T snv 4.0E-02 4.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs41266779
rs41266779 		6 26021644 upstream gene variant C/T snv 4.0E-02 4.3E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs9467664
rs9467664 		0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2009 2009
dbSNP: rs9467664
rs9467664 		0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2009 2009
dbSNP: rs9467664
rs9467664 		0.925 0.120 6 26021585 upstream gene variant A/T snv 0.76
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs759927375
rs759927375 		0.925 0.040 6 26020589 missense variant G/A;C snv 1.2E-05; 8.0E-06
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs759927375
rs759927375 		0.925 0.040 6 26020589 missense variant G/A;C snv 1.2E-05; 8.0E-06
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2013 2013