List of variants in gene RNF213 reported as benign for cardiovascular disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001256071.3(RNF213):c.14194A>G (p.Lys4732Glu)	rs12944385	0.00750
NM_001256071.3(RNF213):c.12942+97del	rs142169239

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