CXCR1, C-X-C motif chemokine receptor 1, 3577

N. diseases: 167; N. variants: 3
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: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0033845
Disease: Pseudotumor Cerebri
Pseudotumor Cerebri 		Nervous System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection 		Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases 0.020 0.500 2 2018 2019
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2013 2013
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2013 2013
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis 		Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2234671
rs2234671 		0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral 		Infections 0.010 1.000 1 2011 2011
dbSNP: rs2671222
rs2671222 		1.000 0.040 2 218167879 upstream gene variant T/C snv 0.89
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2671222
rs2671222 		1.000 0.040 2 218167879 upstream gene variant T/C snv 0.89
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3138060
rs3138060 		1.000 0.040 2 218166777 intron variant G/C snv 7.1E-02
CUI: C0023290
Disease: Leishmaniasis, Visceral
Leishmaniasis, Visceral 		Infections 0.010 1.000 1 2011 2011