GPX3, glutathione peroxidase 3, 2878

N. diseases: 156; N. variants: 6
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: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
Differentiated Thyroid Gland Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
Primary differentiated carcinoma of thyroid gland
0.010 1.000 1 2009 2009
dbSNP: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2070593
rs2070593
0.827 0.120 5 151028379 3 prime UTR variant G/A;T snv 0.20
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3805435
rs3805435
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02
Primary differentiated carcinoma of thyroid gland
0.010 1.000 1 2009 2009
dbSNP: rs3805435
rs3805435
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3805435
rs3805435
0.882 0.120 5 151021735 non coding transcript exon variant T/C snv 8.4E-02
Differentiated Thyroid Gland Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs3828599
rs3828599
0.882 0.040 5 151022235 intron variant A/G snv 0.67
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3828599
rs3828599
0.882 0.040 5 151022235 intron variant A/G snv 0.67
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3828599
rs3828599
0.882 0.040 5 151022235 intron variant A/G snv 0.67
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3828599
rs3828599
0.882 0.040 5 151022235 intron variant A/G snv 0.67
Differentiated Thyroid Gland Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs3828599
rs3828599
0.882 0.040 5 151022235 intron variant A/G snv 0.67
Primary differentiated carcinoma of thyroid gland
0.010 1.000 1 2009 2009
dbSNP: rs8177409
rs8177409
1.000 0.040 5 151020289 upstream gene variant A/T snv 0.15
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs8177412
rs8177412
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs8177412
rs8177412
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15
CUI: C1112433
Disease: Thromboembolic stroke
Thromboembolic stroke
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs8177412
rs8177412
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15
Differentiated Thyroid Gland Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs8177412
rs8177412
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs8177412
rs8177412
0.851 0.160 5 151020526 5 prime UTR variant T/C snv 0.15
Primary differentiated carcinoma of thyroid gland
0.010 1.000 1 2009 2009
dbSNP: rs8177441
rs8177441
1.000 0.040 5 151026433 intron variant G/C snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016