TBL2, transducin beta like 2, 26608

N. diseases: 190; 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: rs35348663
rs35348663 		7 73577263 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35624969
rs35624969 		7 73577262 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 9 2008 2019
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2010 2019
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2010 2013
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.710 1.000 2 2014 2017
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs17145738
rs17145738 		0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs13246490
rs13246490 		7 73578020 3 prime UTR variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13232120
rs13232120 		0.925 0.120 7 73568980 3 prime UTR variant A/T snv 0.11
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs35659126
rs35659126 		7 73573739 intron variant C/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11974409
rs11974409 		0.925 0.120 7 73575060 intron variant A/G snv 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2009 2012
dbSNP: rs11974409
rs11974409 		0.925 0.120 7 73575060 intron variant A/G snv 0.16
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11974409
rs11974409 		0.925 0.120 7 73575060 intron variant A/G snv 0.16
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11974409
rs11974409 		0.925 0.120 7 73575060 intron variant A/G snv 0.16
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012