RETN, resistin, 56729

N. diseases: 302; N. variants: 13
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: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C2699063
Disease: Resistin Measurement
Resistin Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs34124816
rs34124816 		19 7668790 upstream gene variant A/C snv 5.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3745367
rs3745367 		0.827 0.200 19 7669625 intron variant G/A snv 0.39
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia 		0.010 1.000 1 2017 2017
dbSNP: rs750359414
rs750359414 		0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2003 2005
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs750359414
rs750359414 		0.851 0.240 19 7669884 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs3219177
rs3219177 		0.925 0.120 19 7669483 intron variant C/T snv 0.20 0.19
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs3745367
rs3745367 		0.827 0.200 19 7669625 intron variant G/A snv 0.39
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2009 2014
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs769389061
rs769389061 		0.925 0.120 19 7670321 missense variant G/A;C snv
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs3745367
rs3745367 		0.827 0.200 19 7669625 intron variant G/A snv 0.39
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs3745367
rs3745367 		0.827 0.200 19 7669625 intron variant G/A snv 0.39
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 < 0.001 1 2018 2018
dbSNP: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2011 2011
dbSNP: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
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: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3219175
rs3219175 		0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1862513
rs1862513 		0.763 0.360 19 7668907 upstream gene variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs3745367
rs3745367 		0.827 0.200 19 7669625 intron variant G/A snv 0.39
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014