List of variants in gene MEFV reported as likely benign 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: 30

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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.42G>A (p.Glu14=)	rs113314808	0.00369
NM_000243.3(MEFV):c.1467G>A (p.Gln489=)	rs61732424	0.00341
NM_000243.3(MEFV):c.333G>A (p.Gly111=)	rs61732425	0.00339
NM_000243.3(MEFV):c.910G>A (p.Gly304Arg)	rs75977701	0.00316
NM_000243.3(MEFV):c.-15C>G	rs11466015	0.00306
NM_000243.3(MEFV):c.1587+18C>T	rs11466030	0.00248
NM_000243.3(MEFV):c.986G>A (p.Arg329His)	rs104895112	0.00133
NM_000243.3(MEFV):c.932C>T (p.Ala311Val)	rs74346519	0.00063
NM_000243.3(MEFV):c.372C>T (p.Pro124=)	rs104895078	0.00035
NM_000243.3(MEFV):c.1245C>T (p.Val415=)	rs104895195	0.00017
NM_000243.3(MEFV):c.297C>T (p.Asn99=)	rs104895175	0.00016
NM_000243.3(MEFV):c.1518C>T (p.Ile506=)	rs104895099	0.00015
NM_000243.3(MEFV):c.198C>T (p.Ala66=)	rs149380763	0.00009
NM_000243.3(MEFV):c.549G>A (p.Pro183=)	rs587781035	0.00006
NM_000243.3(MEFV):c.657C>T (p.Gly219=)	rs104895182	0.00006
NM_000243.3(MEFV):c.1179C>T (p.Pro393=)	rs104895082	0.00003
NM_000243.3(MEFV):c.195C>T (p.Tyr65=)	rs104895077	0.00003
NM_000243.3(MEFV):c.2169C>T (p.Asp723=)	rs104895117	0.00001
NM_000243.3(MEFV):c.359C>T (p.Thr120Ile)	rs772698222	0.00001
NM_000243.3(MEFV):c.540G>C (p.Pro180=)	rs104895139	0.00001
NM_000243.3(MEFV):c.621C>T (p.Ala207=)	rs767667206	0.00001
NM_000243.3(MEFV):c.1318C>G (p.Gln440Glu)	rs11466026
NM_000243.3(MEFV):c.2253C>G (p.Pro751=)	rs1489831475
NM_000243.3(MEFV):c.2271C>T (p.Ser757=)	rs772754956
NM_000243.3(MEFV):c.330G>A (p.Leu110=)	rs104895177
NM_000243.3(MEFV):c.564C>G (p.Pro188=)	rs775755423
NM_000243.3(MEFV):c.585G>A (p.Glu195=)	rs200766991
NM_000243.3(MEFV):c.699G>A (p.Leu233=)	rs2141676964

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