CORIN, corin, serine peptidase, 10699

N. diseases: 55; N. variants: 9
Disease: Hypertensive disease ×
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: rs111253292
rs111253292 		4 47661743 missense variant T/G snv 4.6E-03 2.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.030 1.000 3 2007 2012
dbSNP: rs75770792
rs75770792 		4 47661782 missense variant G/A snv 4.6E-03 2.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.030 1.000 3 2007 2012
dbSNP: rs2271037
rs2271037 		4 47678068 intron variant T/C;G snv 4.0E-06; 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3749585
rs3749585 		4 47595573 3 prime UTR variant A/G snv 0.11
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018