List of variants in gene MEFV reported by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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.442G>C (p.Glu148Gln)	rs3743930	0.02112
NM_000243.3(MEFV):c.97G>T (p.Val33Leu)	rs11466016	0.00250
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.277+6C>T	rs7199464	0.00071
NM_000243.3(MEFV):c.1151T>C (p.Leu384Pro)	rs139313647	0.00047
NM_000243.3(MEFV):c.1260+10C>T	rs104895137	0.00035
NM_000243.3(MEFV):c.1370C>T (p.Ala457Val)	rs104895151	0.00020
NM_000243.3(MEFV):c.1131C>T (p.Arg377=)	rs149941578	0.00001
NM_000243.3(MEFV):c.688G>A (p.Glu230Lys)	rs104895080	0.00001
NM_000243.3(MEFV):c.1318C>G (p.Gln440Glu)	rs11466026
NM_000243.3(MEFV):c.2230G>T (p.Ala744Ser)	rs61732874
NM_000243.3(MEFV):c.357G>C (p.Lys119Asn)	rs1000657059
NM_000243.3(MEFV):c.941_942delinsAT (p.Arg314His)	rs1085307824

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