SELENOP, selenoprotein P, 6414

N. diseases: 138; 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: rs146689548
rs146689548 		5 42822843 intron variant T/C snv 8.4E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2010 2014
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2010 2014
dbSNP: rs13154178
rs13154178 		5 42827999 intron variant G/A snv 0.31
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs13168440
rs13168440 		0.925 0.080 5 42804013 intron variant T/C snv 0.14
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs13168440
rs13168440 		0.925 0.080 5 42804013 intron variant T/C snv 0.14
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C1306762
Disease: Aortoiliac occlusive disease
Aortoiliac occlusive disease 		0.010 1.000 1 2014 2014
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 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: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3877899
rs3877899 		0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6865453
rs6865453 		5 42810037 intron variant A/C snv 0.22
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2010 2010
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs7579
rs7579 		0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26
CUI: C1306762
Disease: Aortoiliac occlusive disease
Aortoiliac occlusive disease 		0.010 1.000 1 2014 2014