List of variants in gene MEFV reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000243.3(MEFV):c.1506_1507dup (p.Ser503fs)	rs751375381
NM_000243.3(MEFV):c.726C>A (p.Ser242Arg)	rs104895127
NM_000243.3(MEFV):c.761_764dup (p.Asn256fs)	rs104895138

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