List of variants in gene combination CAV3, OXTR reported as likely benign for caveolinopathy

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_033337.3(CAV3):c.166G>A (p.Gly56Ser)	rs72546667	0.03558
NM_033337.3(CAV3):c.171G>A (p.Val57=)	rs61147808	0.01628
NM_033337.2(CAV3):c.216C>G (p.Cys72Trp)	rs116840776	0.00164
NM_033337.3(CAV3):c.*813del	rs66667169

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