List of variants in gene MEFV reported as benign for not specified

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: 33

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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.1428A>G (p.Gln476=)	rs224207	0.58038
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.1105C>T (p.Pro369Ser)	rs11466023	0.01590
NM_000243.3(MEFV):c.1223G>A (p.Arg408Gln)	rs11466024	0.01456
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.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.97G>T (p.Val33Leu)	rs11466016	0.00250
NM_000243.3(MEFV):c.329T>C (p.Leu110Pro)	rs11466018	0.00217
NM_000243.3(MEFV):c.1260+10C>T	rs104895137	0.00035
NM_000243.3(MEFV):c.1245C>T (p.Val415=)	rs104895195	0.00017
NM_000243.3(MEFV):c.1518C>T (p.Ile506=)	rs104895099	0.00015
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.1356+12G>C	rs587781036
NM_000243.3(MEFV):c.414A>G (p.Gly138=)	rs224224
NM_000243.3(MEFV):c.585G>A (p.Glu195=)	rs200766991
NM_000243.3(MEFV):c.586G>T (p.Gly196Trp)	rs104895179
NM_000243.3(MEFV):c.911-2117T>C

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