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: rs2397084
rs2397084 		0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		0.010 1.000 1 2015 2015
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2013 2013
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2017 2017
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		0.010 1.000 1 2015 2015
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: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C1277187
Disease: Left ventricular systolic dysfunction
Left ventricular systolic dysfunction 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 < 0.001 1 2015 2015
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: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.030 0.667 3 2008 2013
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2008 2013
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.020 0.500 2 2008 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: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0013289
Disease: Duodenal Diseases
Duodenal Diseases 		Digestive System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer 		Digestive System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases 		Digestive System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.100 0.700 10 2014 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.100 0.700 10 2014 2019
dbSNP: rs763780
rs763780 		0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.040 1.000 4 2015 2019
dbSNP: rs2397084
rs2397084 		0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
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: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015