List of variants in gene MEFV reported by Mayo Clinic Laboratories, Mayo Clinic

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000243.3(MEFV):c.1105C>T (p.Pro369Ser)	rs11466023	0.01590
NM_000243.3(MEFV):c.1223G>A (p.Arg408Gln)	rs11466024	0.01456
NM_000243.3(MEFV):c.97G>T (p.Val33Leu)	rs11466016	0.00250
NM_000243.3(MEFV):c.1459G>C (p.Val487Leu)	rs104895100	0.00207
NM_000243.3(MEFV):c.2177T>C (p.Val726Ala)	rs28940579	0.00147
NM_000243.3(MEFV):c.986G>A (p.Arg329His)	rs104895112	0.00133
NM_000243.3(MEFV):c.1341G>C (p.Lys447Asn)	rs756322372	0.00011
NM_000243.3(MEFV):c.1060C>T (p.Arg354Trp)	rs104895116	0.00004
NM_000243.3(MEFV):c.277G>C (p.Glu93Gln)	rs138498376	0.00004
NM_000243.3(MEFV):c.611G>A (p.Arg204His)	rs775663363	0.00004
NM_000243.3(MEFV):c.941G>A (p.Arg314His)	rs104895204	0.00004
NM_000243.3(MEFV):c.536G>A (p.Ser179Asn)	rs104895125	0.00001
NM_000243.3(MEFV):c.553G>A (p.Gly185Arg)	rs1266566289	0.00001
NM_000243.3(MEFV):c.2230G>T (p.Ala744Ser)	rs61732874

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