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: rs1889570
rs1889570 		0.882 0.160 6 52245936 upstream gene variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.030 1.000 3 2011 2015
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: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases 		Digestive System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12203582
rs12203582 		0.827 0.120 6 52240759 intron variant G/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
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: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
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: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2015 2015
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
dbSNP: rs1266828
rs1266828 		0.807 0.120 6 52243264 intron variant G/A snv 0.75
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma 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: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2015 2015
dbSNP: rs1266828
rs1266828 		0.807 0.120 6 52243264 intron variant G/A snv 0.75
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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 < 0.001 1 2015 2015
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: 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: rs9382084
rs9382084 		0.925 0.080 6 52240869 intron variant G/A;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9382084
rs9382084 		0.925 0.080 6 52240869 intron variant G/A;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9463772
rs9463772 		0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs9463772
rs9463772 		0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs9463772
rs9463772 		0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs748486078
rs748486078 		1.000 6 52237139 missense variant G/A snv 4.4E-05 5.6E-05
CUI: C3151405
Disease: CANDIDIASIS, FAMILIAL, 6
CANDIDIASIS, FAMILIAL, 6 		0.800 0
dbSNP: rs11465553
rs11465553 		0.925 0.120 6 52236960 missense variant C/T snv 3.0E-02 3.0E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11465553
rs11465553 		0.925 0.120 6 52236960 missense variant C/T snv 3.0E-02 3.0E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2011 2011