C0085077[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 97509	NM_000243.3(MEFV):c.2314A>G (p.Ile772Val)	MEFV (I772V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 1018295	NM_000243.3(MEFV):c.2310_2313del (p.Thr771fs)	MEFV (T771fs)	Deletion (frameshift variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 2549	NM_000243.3(MEFV):c.2282G>A (p.Arg761His)	MEFV (R761H)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +5 more	GPathogenic/Likely pathogenic
Select item 495753	NM_000243.3(MEFV):c.2271C>T (p.Ser757=)	MEFV	Single nucleotide variant (synonymous variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 97507	NM_000243.3(MEFV):c.2263A>G (p.Ile755Val)	MEFV (I755V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 97505	NM_000243.3(MEFV):c.2246C>G (p.Ser749Cys)	MEFV (S749C)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +4 more	GConflicting classifications of pathogenicity
Select item 2548	NM_000243.3(MEFV):c.2230G>T (p.Ala744Ser)	MEFV	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 97503	NM_000243.3(MEFV):c.2229C>G (p.Phe743Leu)	MEFV (F743L)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 2540	NM_000243.3(MEFV):c.2177T>C (p.Val726Ala)	MEFV (V726A)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +5 more	GPathogenic/Likely pathogenic
Select item 803178	NM_000243.3(MEFV):c.2150G>A (p.Arg717His)	LOC126862264, MEFV (R717H)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 803177	NM_000243.3(MEFV):c.2150G>T (p.Arg717Leu)	LOC126862264, MEFV (R717L)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 234551	NM_000243.3(MEFV):c.2141C>T (p.Pro714Leu)	LOC126862264, MEFV (P714L)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 649340	NM_000243.3(MEFV):c.2123G>A (p.Arg708His)	LOC126862264, MEFV (R708H)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 970490	NM_000243.3(MEFV):c.2117C>T (p.Pro706Leu)	LOC126862264, MEFV (P706L)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 845727	NM_000243.3(MEFV):c.2111T>G (p.Val704Gly)	LOC126862264, MEFV (V704G)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 97493	NM_000243.3(MEFV):c.2109C>T (p.Ser703=)	LOC126862264, MEFV	Single nucleotide variant (synonymous variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 2538	NM_000243.3(MEFV):c.2080A>G (p.Met694Val)	LOC126862264, MEFV	Single nucleotide variant (missense variant +1 more)	Recurrent fever +24 more	GPathogenic/Likely pathogenic
Select item 1478684	NM_000243.3(MEFV):c.2078T>C (p.Met693Thr)	LOC126862264, MEFV (M693T)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 888112	NM_000243.3(MEFV):c.2068G>C (p.Val690Leu)	LOC126862264, MEFV (V690L)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 859245	NM_000243.3(MEFV):c.2065T>C (p.Trp689Arg)	LOC126862264, MEFV (W689R)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 577934	NM_000243.3(MEFV):c.2044_2045del (p.Leu682fs)	LOC126862264, MEFV (L682fs)	Microsatellite (frameshift variant +1 more)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 36507	NM_000243.3(MEFV):c.2040G>C (p.Met680Ile)	LOC126862264, MEFV	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +6 more	GPathogenic
Select item 97479	NM_000243.3(MEFV):c.2033G>A (p.Gly678Glu)	LOC126862264, MEFV (G678E)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 811766	NM_000243.3(MEFV):c.1996A>T (p.Ile666Phe)	LOC126862264, MEFV (I666F)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 1062670	NM_000243.3(MEFV):c.1957C>A (p.Arg653Ser)	LOC126862264, MEFV (R653S)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 793936	NM_000243.3(MEFV):c.1899G>A (p.Pro633=)	LOC126862264, MEFV	Single nucleotide variant (synonymous variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 457998	NM_000243.3(MEFV):c.1898C>T (p.Pro633Leu)	LOC126862264, MEFV (P633L)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 97467	NM_000243.3(MEFV):c.1894G>A (p.Gly632Ser)	LOC126862264, MEFV (G632S)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 803182	NM_000243.3(MEFV):c.1889C>T (p.Pro630Leu)	LOC126862264, MEFV (P630L)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 234364	NM_000243.3(MEFV):c.1886dup (p.Pro630fs)	LOC126862264, MEFV (P630fs)	Duplication (frameshift variant +1 more)	Familial Mediterranean fever, autosomal dominant +4 more	GConflicting classifications of pathogenicity
Select item 97464	NM_000243.3(MEFV):c.1795A>G (p.Asn599Asp)	LOC126862264, MEFV (N599D)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 527802	NM_000243.3(MEFV):c.1780C>T (p.Gln594Ter)	LOC126862264, MEFV (Q594* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 992257	NM_000243.3(MEFV):c.1759+12G>A	LOC126862264, MEFV	Single nucleotide variant (intron variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 439888	NM_000243.3(MEFV):c.1759+11C>T	LOC126862264, MEFV	Single nucleotide variant (intron variant)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 97456	NM_000243.3(MEFV):c.1744A>C (p.Met582Leu)	LOC126862264, MEFV (M582L +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +4 more	GConflicting classifications of pathogenicity
Select item 319109	NM_000243.3(MEFV):c.1736G>A (p.Arg579His)	LOC126862264, MEFV (R579H +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +3 more	GUncertain significance
Select item 1467370	NM_000243.3(MEFV):c.1685A>G (p.Gln562Arg)	LOC126862264, MEFV (Q351R +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 864685	NM_000243.3(MEFV):c.1681C>T (p.His561Tyr)	LOC126862264, MEFV (H561Y +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 495752	NM_000243.3(MEFV):c.1622T>C (p.Val541Ala)	MEFV (V541A +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 439886	NM_000243.3(MEFV):c.1610+8G>A	MEFV	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1179055	NM_000243.3(MEFV):c.1597_1598dup (p.Asp533fs)	MEFV (D322fs +1 more)	Microsatellite (frameshift variant)	Familial Mediterranean fever +2 more	GLikely pathogenic
Select item 1122743	NM_000243.3(MEFV):c.1533G>A (p.Ala511=)	MEFV	Single nucleotide variant (synonymous variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 646921	NM_000243.3(MEFV):c.1532C>T (p.Ala511Val)	MEFV (A511V +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 955767	NM_000243.3(MEFV):c.1528G>A (p.Asp510Asn)	MEFV (D299N +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 319112	NM_000243.3(MEFV):c.1513G>T (p.Asp505Tyr)	MEFV (D505Y +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 1179060	NM_000243.3(MEFV):c.1510C>T (p.Gln504Ter)	MEFV (Q293* +1 more)	Single nucleotide variant (nonsense)	Familial Mediterranean fever +2 more	GPathogenic
Select item 457996	NM_000243.3(MEFV):c.1508C>G (p.Ser503Cys)	MEFV (S503C +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +4 more	GConflicting classifications of pathogenicity
Select item 527800	NM_000243.3(MEFV):c.1504G>A (p.Val502Ile)	MEFV (V502I +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 918136	NM_000243.3(MEFV):c.1501C>T (p.Arg501Cys)	MEFV (R290C +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 97447	NM_000243.3(MEFV):c.1501C>G (p.Arg501Gly)	MEFV (R501G +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 97445	NM_000243.3(MEFV):c.1459G>A (p.Val487Met)	MEFV (V487M +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 319113	NM_000243.3(MEFV):c.1406T>C (p.Val469Ala)	MEFV (V469A +1 more)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 1157571	NM_000243.3(MEFV):c.1401G>A (p.Glu467=)	MEFV	Single nucleotide variant (synonymous variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 761100	NM_000243.3(MEFV):c.1344A>C (p.Ala448=)	MEFV	Single nucleotide variant (synonymous variant)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 279849	NM_000243.3(MEFV):c.1341G>C (p.Lys447Asn)	MEFV (K447N +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +4 more	GConflicting classifications of pathogenicity
Select item 234502	NM_000243.3(MEFV):c.1337A>C (p.Glu446Ala)	MEFV (E446A +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 945593	NM_000243.3(MEFV):c.1324T>A (p.Ser442Thr)	MEFV (S231T +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 457995	NM_000243.3(MEFV):c.1223G>T (p.Arg408Leu)	MEFV (R408L +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +4 more	GConflicting classifications of pathogenicity
Select item 457994	NM_000243.3(MEFV):c.1222C>T (p.Arg408Trp)	MEFV (R408W +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 97434	NM_000243.3(MEFV):c.1179C>T (p.Pro393=)	MEFV	Single nucleotide variant (synonymous variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 450568	NM_000243.3(MEFV):c.1171G>A (p.Asp391Asn)	MEFV (D391N +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +3 more	GConflicting classifications of pathogenicity
Select item 663143	NM_000243.3(MEFV):c.1151T>C (p.Leu384Pro)	MEFV (L384P +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 888171	NM_000243.3(MEFV):c.1105C>A (p.Pro369Thr)	MEFV (P369T +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 375253	NM_000243.3(MEFV):c.1099C>G (p.Leu367Val)	MEFV (L367V +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +4 more	GConflicting classifications of pathogenicity
Select item 527806	NM_000243.3(MEFV):c.1092G>A (p.Pro364=)	MEFV	Single nucleotide variant (synonymous variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 97432	NM_000243.3(MEFV):c.1091C>T (p.Pro364Leu)	MEFV (P364L +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 160359	NM_000243.3(MEFV):c.1082G>C (p.Arg361Thr)	MEFV (R361T +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 234501	NM_000243.3(MEFV):c.1066C>G (p.Gln356Glu)	MEFV (Q356E +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 495749	NM_000243.3(MEFV):c.1061G>A (p.Arg354Gln)	MEFV (R354Q +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 97430	NM_000243.3(MEFV):c.1060C>T (p.Arg354Trp)	MEFV (R354W +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 1385081	NM_000243.3(MEFV):c.985C>T (p.Arg329Cys)	MEFV (R329C +1 more)	Single nucleotide variant (missense variant)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 853724	NM_000243.3(MEFV):c.973G>A (p.Gly325Ser)	MEFV (G114S +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 234361	NM_000243.3(MEFV):c.959G>C (p.Gly320Ala)	MEFV (G320A +1 more)	Single nucleotide variant (missense variant)	Familial Mediterranean fever, autosomal dominant +3 more	GConflicting classifications of pathogenicity
Select item 1674612	NM_000243.3(MEFV):c.933G>A (p.Ala311=)	MEFV	Single nucleotide variant (synonymous variant)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 97550	NM_000243.3(MEFV):c.866C>T (p.Ala289Val)	MEFV (A289V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +5 more	GConflicting classifications of pathogenicity
Select item 56152	NM_000243.3(MEFV):c.863C>A (p.Ser288Tyr)	MEFV (S288Y)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 97549	NM_000243.3(MEFV):c.848C>T (p.Pro283Leu)	MEFV (P283L)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 97548	NM_000243.3(MEFV):c.848C>G (p.Pro283Arg)	MEFV (P283R)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 848470	NM_000243.3(MEFV):c.828A>C (p.Glu276Asp)	MEFV (E276D)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 870681	NM_000243.3(MEFV):c.808A>G (p.Asn270Asp)	MEFV (N270D)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 97546	NM_000243.3(MEFV):c.803C>T (p.Ala268Val)	MEFV (A268V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 97545	NM_000243.3(MEFV):c.775A>G (p.Ile259Val)	MEFV (I259V)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever, autosomal dominant +6 more	GConflicting classifications of pathogenicity
Select item 1140278	NM_000243.3(MEFV):c.765A>G (p.Ala255=)	MEFV	Single nucleotide variant (synonymous variant +1 more)	Familial Mediterranean fever, autosomal dominant +2 more	GConflicting classifications of pathogenicity
Select item 1315983	NM_000243.3(MEFV):c.656G>A (p.Gly219Asp)	MEFV (G219D)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 651794	NM_000243.3(MEFV):c.586G>C (p.Gly196Arg)	MEFV (G196R)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +2 more	GConflicting classifications of pathogenicity
Select item 965372	NM_000243.3(MEFV):c.565_570dup (p.Gly189_Pro190dup)	MEFV	Duplication (inframe_insertion +1 more)	Familial Mediterranean fever, autosomal dominant +4 more	GConflicting classifications of pathogenicity
Select item 953572	NM_000243.3(MEFV):c.566G>T (p.Gly189Val)	MEFV (G189V)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 850658	NM_000243.3(MEFV):c.548C>T (p.Pro183Leu)	MEFV (P183L)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 234358	NM_000243.3(MEFV):c.547C>A (p.Pro183Thr)	MEFV (P183T)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever, autosomal dominant +4 more	GConflicting classifications of pathogenicity
Select item 450323	NM_000243.3(MEFV):c.532C>T (p.Arg178Trp)	MEFV (R178W)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +3 more	GConflicting classifications of pathogenicity
Select item 97527	NM_000243.3(MEFV):c.524C>A (p.Pro175His)	MEFV (P175H)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +4 more	GConflicting classifications of pathogenicity
Select item 1006519	NM_000243.3(MEFV):c.520A>G (p.Lys174Glu)	MEFV (K174E)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 966080	NM_000243.3(MEFV):c.497C>T (p.Ser166Leu)	MEFV (S166L)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever, autosomal dominant +3 more	GConflicting classifications of pathogenicity
Select item 811962	NM_000243.3(MEFV):c.490A>C (p.Lys164Gln)	MEFV (K164Q)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +3 more	GConflicting classifications of pathogenicity
Select item 392469	NM_000243.3(MEFV):c.489G>T (p.Glu163Asp)	MEFV (E163D)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1011684	NM_000243.3(MEFV):c.475A>G (p.Ser159Gly)	MEFV (S159G)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 234355	NM_000243.3(MEFV):c.460T>C (p.Ser154Pro)	MEFV (S154P)	Single nucleotide variant (missense variant +1 more)	Familial Mediterranean fever +4 more	GConflicting classifications of pathogenicity
Select item 756743	NM_000243.3(MEFV):c.456G>A (p.Gly152=)	MEFV	Single nucleotide variant (synonymous variant +1 more)	Acute febrile neutrophilic dermatosis +2 more	GConflicting classifications of pathogenicity
Select item 2554	NM_000243.3(MEFV):c.443A>T (p.Glu148Val)	MEFV (E148V)	Single nucleotide variant (missense variant +1 more)	Acute febrile neutrophilic dermatosis +5 more	GConflicting classifications of pathogenicity
Select item 234353	NM_000243.3(MEFV):c.439C>G (p.Pro147Ala)	MEFV (P147A)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity

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