List of variants in gene combination CAV3, OXTR reported as benign for hereditary skeletal muscle 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_033337.3(CAV3):c.123T>C (p.Phe41=)	rs13087941	0.23875
NM_033337.3(CAV3):c.166G>A (p.Gly56Ser)	rs72546667	0.03558

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