ClinVar Miner

Submissions for variant NM_014336.5(AIPL1):c.33G>C (p.Gly11=)

gnomAD frequency: 0.00001  dbSNP: rs369223841
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000950571 SCV001096895 likely benign Leber congenital amaurosis 4 2024-01-25 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001123502 SCV001282343 uncertain significance Retinitis pigmentosa 2017-04-28 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Illumina Laboratory Services, Illumina RCV000950571 SCV001282344 uncertain significance Leber congenital amaurosis 4 2017-04-28 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases did not allow this variant to be ruled in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

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