ClinVar Miner

Submissions for variant NM_002900.3(RBP3):c.924G>A (p.Pro308=)

gnomAD frequency: 0.00317  dbSNP: rs35746996
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000889648 SCV001033346 benign not provided 2024-01-19 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001105737 SCV001262734 benign 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). Publications were found based on this search. The evidence from the literature, in combination with allele frequency data from public databases where available, was sufficient to rule this variant out of causing disease. Therefore, this variant is classified as benign.

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