ClinVar Miner

List of variants in gene combination FECH, LOC130062554 reported as uncertain significance for porphyria

Included ClinVar conditions (23):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000140.5(FECH):c.*5090G>A	rs776370345	0.00060
NM_000140.5(FECH):c.*5170T>C	rs886053966

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