ClinVar Miner

Submissions for variant NM_000146.4(FTL):c.-167C>T

dbSNP: rs2038438402
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001238029 SCV001410823 pathogenic Hereditary hyperferritinemia with congenital cataracts; Neuroferritinopathy 2024-01-16 criteria provided, single submitter clinical testing This variant occurs in a non-coding region of the FTL gene. It does not change the encoded amino acid sequence of the FTL protein. This variant is not present in population databases (gnomAD no frequency). This variant has been observed in individuals with hereditary hyperferritinemia cataract syndrome (PMID: 16900584, 19800271, 22881709, 27096259). It has also been observed to segregate with disease in related individuals. This variant is also known as +33C>U or +33C>T. ClinVar contains an entry for this variant (Variation ID: 963917). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. For these reasons, this variant has been classified as Pathogenic.
MGZ Medical Genetics Center RCV002290654 SCV002578921 pathogenic Hereditary hyperferritinemia with congenital cataracts 2022-03-15 criteria provided, single submitter clinical testing

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