POSTN, periostin, 10631

N. diseases: 378; N. variants: 4
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: rs117103342
rs117103342 		13 37582401 missense variant C/T snv 4.4E-03 5.1E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1028728
rs1028728 		0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1028728
rs1028728 		0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1028728
rs1028728 		0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1449599973
rs1449599973 		1.000 0.080 13 37587856 missense variant T/C snv 4.0E-06
CUI: C0008928
Disease: Cleidocranial Dysplasia
Cleidocranial Dysplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 1997 1997
dbSNP: rs3829365
rs3829365 		0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3829365
rs3829365 		0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3829365
rs3829365 		0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2011 2011