List of variants in gene CORIN studied for hypertensive disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006587.4(CORIN):c.2047A>T (p.Ser683Cys)	rs144722161	0.00222
NM_006587.4(CORIN):c.1414A>G (p.Ser472Gly)	rs387906895
NM_006587.4(CORIN):c.684dup (p.Met229fs)	rs756399499
NM_006587.4(CORIN):c.949A>G (p.Lys317Glu)	rs387906894

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