IL17F, interleukin 17F, 112744

N. diseases: 236; N. variants: 10
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: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.040 1.000 4 2019 2019
dbSNP: rs1889570
rs1889570 		0.882 0.160 6 52245936 upstream gene variant C/A;T snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2397084
rs2397084 		0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0012243
Disease: Digestive System Neoplasms
Digestive System Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0017657
Disease: Glomerulitis (disorder)
Glomerulitis (disorder) 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0026269
Disease: Mitral Valve Stenosis
Mitral Valve Stenosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.020 1.000 2 2018 2019
dbSNP: rs1889570
rs1889570 		0.882 0.160 6 52245936 upstream gene variant C/A;T snv
CUI: C0014038
Disease: Encephalitis
Encephalitis 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs376671742
rs376671742 		1.000 0.040 6 52238749 missense variant T/A;G snv
CUI: C2937365
Disease: Recurrent aphthous ulcer
Recurrent aphthous ulcer 		Stomatognathic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		Skin and Connective Tissue Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease 		Infections; Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2017 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0272286
Disease: Thrombocytopenia due to platelet alloimmunization
Thrombocytopenia due to platelet alloimmunization 		Hemic and Lymphatic Diseases 0.020 1.000 2 2017 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0242584
Disease: Autoimmune thrombocytopenia
Autoimmune thrombocytopenia 		Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2017 2019
dbSNP: rs12203582
rs12203582 		0.827 0.120 6 52240759 intron variant G/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12203582
rs12203582 		0.827 0.120 6 52240759 intron variant G/A;T snv
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs12203582
rs12203582 		0.827 0.120 6 52240759 intron variant G/A;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12203582
rs12203582 		0.827 0.120 6 52240759 intron variant G/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1266828
rs1266828 		0.807 0.120 6 52243264 intron variant G/A snv 0.75
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017