ClinVar Miner

Submissions for variant NM_000140.5(FECH):c.*4829C>T

gnomAD frequency: 0.00093  dbSNP: rs565989254
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000382609 SCV000409563 likely benign Protoporphyria, erythropoietic, 1 2016-06-14 criteria provided, single submitter clinical testing

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