List of variants in gene MEFV reported as benign by GeneDx

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: 51

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HGVS	dbSNP	gnomAD frequency
NM_000243.3(MEFV):c.942C>T (p.Arg314=)	rs224213	0.61317
NM_000243.3(MEFV):c.1356+267C>T	rs224211	0.59651
NM_000243.3(MEFV):c.1356+44A>G	rs224212	0.59650
NM_000243.3(MEFV):c.1530T>C (p.Asp510=)	rs224206	0.59561
NM_000243.3(MEFV):c.*267G>A	rs2741918	0.58813
NM_000243.3(MEFV):c.*245G>A	rs2741919	0.58215
NM_000243.3(MEFV):c.1428A>G (p.Gln476=)	rs224207	0.58038
NM_000243.3(MEFV):c.1611-343T>G	rs170383	0.57940
NM_000243.3(MEFV):c.1422G>A (p.Glu474=)	rs224208	0.57768
NM_000243.3(MEFV):c.306T>C (p.Asp102=)	rs224225	0.48544
NM_000243.3(MEFV):c.495C>A (p.Ala165=)	rs224223	0.48450
NM_000243.3(MEFV):c.1610+96C>T	rs224204	0.46165
NM_000243.3(MEFV):c.1588-69G>A	rs224205	0.46073
NM_000243.3(MEFV):c.1611-90C>T	rs1231124	0.41206
NM_000243.3(MEFV):c.605G>A (p.Arg202Gln)	rs224222	0.20976
NM_000243.3(MEFV):c.1610+186A>G	rs767067	0.11266
NC_000016.10:g.3256757C>T	rs11466014	0.02353
NM_000243.3(MEFV):c.*133G>A	rs2075849	0.01591
NM_000243.3(MEFV):c.1261-11T>G	rs77086855	0.00875
NM_000243.3(MEFV):c.1503C>T (p.Arg501=)	rs76464258	0.00733
NM_000243.3(MEFV):c.*9C>T	rs11466048	0.00618
NM_000243.3(MEFV):c.1260+92G>A	rs104895209	0.00590
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.1587+18C>T	rs11466030	0.00248
NM_000243.3(MEFV):c.329T>C (p.Leu110Pro)	rs11466018	0.00217
NM_000243.3(MEFV):c.1173T>C (p.Asp391=)	rs146077729	0.00201
NM_000243.3(MEFV):c.1610+10G>T	rs11466033	0.00136
NM_000243.3(MEFV):c.1260+10C>T	rs104895137	0.00035
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.1261-28A>G	rs104895140	0.00015
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.663G>C (p.Pro221=)	rs104895162	0.00007
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.948C>T (p.His316=)	rs150252937	0.00004
NM_000243.3(MEFV):c.2166G>A (p.Val722=)	rs762351424	0.00001
NM_000243.3(MEFV):c.48G>A (p.Leu16=)	rs777381107	0.00001
NM_000243.3(MEFV):c.1092G>T (p.Pro364=)	rs11466022
NM_000243.3(MEFV):c.1356+12G>C	rs587781036
NM_000243.3(MEFV):c.1357-306del	rs11466028
NM_000243.3(MEFV):c.411C>G (p.Gly137=)	rs1266277814
NM_000243.3(MEFV):c.414A>G (p.Gly138=)	rs224224
NM_000243.3(MEFV):c.495C>T (p.Ala165=)	rs224223
NM_000243.3(MEFV):c.585G>A (p.Glu195=)	rs200766991
NM_000243.3(MEFV):c.909C>T (p.Thr303=)	rs1429025477
NM_000243.3(MEFV):c.911-23G>A	rs754637045

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