GPC5, glypican 5, 2262

N. diseases: 2; N. variants: 14
Source: CURATED ×
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: rs9523762
rs9523762 		0.925 0.120 13 92679633 intron variant G/A snv 0.39
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.820 1.000 1 2009 2013
dbSNP: rs7982677
rs7982677 		1.000 0.080 13 92336070 intron variant C/A snv 0.29
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.800 1.000 1 2013 2013
dbSNP: rs342702
rs342702 		13 91770692 intron variant G/T snv 0.37
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs138994828
rs138994828 		13 92028205 intron variant G/A snv 5.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1411741
rs1411741 		1.000 0.080 13 92101599 intron variant A/G snv 0.98
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs16946160
rs16946160 		13 91551559 intron variant G/A snv 0.13
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17267292
rs17267292 		13 92670893 intron variant T/C snv 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2008 2008
dbSNP: rs17267292
rs17267292 		13 92670893 intron variant T/C snv 0.22
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2008 2008
dbSNP: rs1929922
rs1929922 		13 91799629 intron variant G/A snv 0.37
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4643170
rs4643170 		13 92713924 intron variant A/C snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4771856
rs4771856 		1.000 0.080 13 92342256 intron variant C/A snv 0.29
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs4771859
rs4771859 		13 92436398 intron variant T/C snv 0.62
CUI: C3548510
Disease: response to antineoplastic agent
response to antineoplastic agent 		0.700 1.000 1 2013 2013
dbSNP: rs7328464
rs7328464 		13 91849410 intron variant C/T snv 0.14
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7981515
rs7981515 		13 91870760 intron variant G/T snv 0.13
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9516053
rs9516053 		1.000 0.120 13 92293631 intron variant T/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2019 2019