C4692546[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 327315	NM_000140.5(FECH):c.*5801T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327316	NM_000140.5(FECH):c.*5628C>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327317	NM_000140.5(FECH):c.*5588G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327318	NM_000140.5(FECH):c.*5394G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327319	NM_000140.5(FECH):c.*5349C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327320	NM_000140.5(FECH):c.*5247T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327321	NM_000140.5(FECH):c.*5170T>C	FECH, LOC130062554	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327322	NM_000140.5(FECH):c.*5143C>T	FECH, LOC130062554	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327323	NM_000140.5(FECH):c.*5140G>A	FECH, LOC130062554	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327324	NM_000140.5(FECH):c.*5139C>T	FECH, LOC130062554	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327325	NM_000140.5(FECH):c.*5090G>A	LOC130062554, FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327326	NM_000140.5(FECH):c.*4971A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327327	NM_000140.5(FECH):c.*4891dup	FECH	Duplication (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327328	NM_000140.5(FECH):c.*4886T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327329	NM_000140.5(FECH):c.4883_4884insC	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327330	NM_000140.5(FECH):c.*4829C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327331	NM_000140.5(FECH):c.*4793TTA[1]	FECH	Microsatellite (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327332	NM_000140.5(FECH):c.*4720T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327333	NM_000140.5(FECH):c.*4598T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327334	NM_000140.5(FECH):c.*4597T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327335	NM_000140.5(FECH):c.*4563G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327336	NM_000140.5(FECH):c.*4528C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327337	NM_000140.5(FECH):c.*4463A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327338	NM_000140.5(FECH):c.*4458C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327339	NM_000140.5(FECH):c.*4449A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327340	NM_000140.5(FECH):c.*4445G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327341	NM_000140.5(FECH):c.*4368G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327342	NM_000140.5(FECH):c.*4367C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327343	NM_000140.5(FECH):c.*4363G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327344	NM_000140.5(FECH):c.*4337G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327345	NM_000140.5(FECH):c.*4336A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327346	NM_000140.5(FECH):c.*4237A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327347	NM_000140.5(FECH):c.*4106A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327348	NM_000140.5(FECH):c.*4077C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327349	NM_000140.5(FECH):c.*4056C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327350	NM_000140.5(FECH):c.*3976C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327351	NM_000140.5(FECH):c.*3841C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327352	NM_000140.5(FECH):c.*3804G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327353	NM_000140.5(FECH):c.*3788A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327354	NM_000140.5(FECH):c.3753_3754insT	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327355	NM_000140.5(FECH):c.*3719C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327356	NM_000140.5(FECH):c.*3716C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327357	NM_000140.5(FECH):c.*3691C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327358	NM_000140.5(FECH):c.*3656C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327359	NM_000140.5(FECH):c.*3601A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327360	NM_000140.5(FECH):c.*3567G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327361	NM_000140.5(FECH):c.*3377G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327362	NM_000140.5(FECH):c.*3339G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327363	NM_000140.5(FECH):c.*3170T>C	FECH, LOC129390998	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327364	NM_000140.5(FECH):c.*3129C>T	FECH, LOC129390998	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327365	NM_000140.5(FECH):c.*2840C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327366	NM_000140.5(FECH):c.*2825A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327367	NM_000140.5(FECH):c.*2788G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327368	NM_000140.5(FECH):c.*2782G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327369	NM_000140.5(FECH):c.*2739T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327370	NM_000140.5(FECH):c.*2644A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327371	NM_000140.5(FECH):c.*2600G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327372	NM_000140.5(FECH):c.*2599C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327373	NM_000140.5(FECH):c.*2526T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327374	NM_000140.5(FECH):c.*2513G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327376	NM_000140.5(FECH):c.2459_2461dup	FECH	Duplication (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327375	NM_000140.5(FECH):c.*2461dup	FECH	Duplication (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327377	NM_000140.5(FECH):c.2451_2452insG	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327379	NM_000140.5(FECH):c.*2451T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327378	NM_000140.5(FECH):c.2450_2451insG	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327380	NM_000140.5(FECH):c.*2436GTTTT[2]	FECH	Microsatellite (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327381	NM_000140.5(FECH):c.*2446G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327382	NM_000140.5(FECH):c.*2443T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327383	NM_000140.5(FECH):c.*2441G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327384	NM_000140.5(FECH):c.*2371T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327385	NM_000140.5(FECH):c.*2079C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327386	NM_000140.5(FECH):c.*2060C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327387	NM_000140.5(FECH):c.*1966G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327388	NM_000140.5(FECH):c.*1950A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327389	NM_000140.5(FECH):c.*1915G>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327390	NM_000140.5(FECH):c.*1622T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327391	NM_000140.5(FECH):c.*1567A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327392	NM_000140.5(FECH):c.*1508G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327393	NM_000140.5(FECH):c.*1479T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327394	NM_000140.5(FECH):c.*1453T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327395	NM_000140.5(FECH):c.*1348T>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327397	NM_000140.5(FECH):c.1287_1288insTTTA	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327396	NM_000140.5(FECH):c.1287_1288insTA	FECH	Insertion (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327398	NM_000140.5(FECH):c.*1287T>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327400	NM_000140.5(FECH):c.*1176G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327399	NM_000140.5(FECH):c.1170_1176delinsAAATCTTCTATGTTTGTATTACTCTCTGGTAA	FECH	Indel (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327401	NM_000140.5(FECH):c.*1175G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327402	NM_000140.5(FECH):c.*1173A>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327403	NM_000140.5(FECH):c.*1170T>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327404	NM_000140.5(FECH):c.*1071C>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327405	NM_000140.5(FECH):c.*1054T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327406	NM_000140.5(FECH):c.*1039G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327407	NM_000140.5(FECH):c.*1032G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327408	NM_000140.5(FECH):c.*936C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327409	NM_000140.5(FECH):c.*892T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327410	NM_000140.5(FECH):c.*825T>C	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GUncertain significance
Select item 327411	NM_000140.5(FECH):c.*696C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign
Select item 327412	NM_000140.5(FECH):c.*592C>T	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327413	NM_000140.5(FECH):c.*571G>A	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GLikely benign
Select item 327414	NM_000140.5(FECH):c.*481A>G	FECH	Single nucleotide variant (3 prime UTR variant)	Protoporphyria, erythropoietic, 1	GBenign

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