CSF2, colony stimulating factor 2, 1437

N. diseases: 1028; N. variants: 7
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: rs1469149
rs1469149
5 132073149 upstream gene variant A/C snv 0.39
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2069639
rs2069639
5 132075408 intron variant A/T snv 1.4E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs25884
rs25884
5 132076545 upstream gene variant A/G snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs25884
rs25884
5 132076545 upstream gene variant A/G snv 0.31
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs747762300
rs747762300
1.000 0.040 5 132074826 missense variant A/C snv 4.0E-06
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode
Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs1426039367
rs1426039367
0.925 0.080 5 132073916 synonymous variant G/A snv 7.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Nutritional and Metabolic Diseases; Nervous System Diseases 0.040 1.000 4 2001 2016
dbSNP: rs1426039367
rs1426039367
0.925 0.080 5 132073916 synonymous variant G/A snv 7.0E-06
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy
0.020 1.000 2 2001 2005
dbSNP: rs25882
rs25882
0.925 0.080 5 132075767 missense variant T/C snv 0.26 0.26
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs25882
rs25882
0.925 0.080 5 132075767 missense variant T/C snv 0.26 0.26
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs753438778
rs753438778
0.925 0.160 5 132074925 missense variant C/G;T snv 8.0E-06; 4.0E-06
Gerstmann-Straussler-Scheinker Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs753438778
rs753438778
0.925 0.160 5 132074925 missense variant C/G;T snv 8.0E-06; 4.0E-06
CUI: C0022336
Disease: Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease
Infections; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013