CSF3, colony stimulating factor 3, 1440

N. diseases: 687; 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: rs146890554
rs146890554 		17 40017384 3 prime UTR variant C/T snv 9.6E-03
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs146890554
rs146890554 		17 40017384 3 prime UTR variant C/T snv 9.6E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs146890554
rs146890554 		17 40017384 3 prime UTR variant C/T snv 9.6E-03
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs146890554
rs146890554 		17 40017384 3 prime UTR variant C/T snv 9.6E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs146890554
rs146890554 		17 40017384 3 prime UTR variant C/T snv 9.6E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs25645
rs25645 		17 40016890 synonymous variant G/A snv 0.39 0.29
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1042658
rs1042658 		1.000 0.080 17 40017649 3 prime UTR variant C/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs757308934
rs757308934 		17 40016599 missense variant G/A snv 9.2E-05 4.9E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2007 2007
dbSNP: rs757308934
rs757308934 		17 40016599 missense variant G/A snv 9.2E-05 4.9E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2007 2007