ClinVar Miner

Submissions for variant NM_003640.5(ELP1):c.1614G>C (p.Met538Ile)

gnomAD frequency: 0.00003  dbSNP: rs749608070
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000290763 SCV000476577 uncertain significance Familial dysautonomia 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
Counsyl RCV000290763 SCV000791963 uncertain significance Familial dysautonomia 2017-06-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001850929 SCV002175063 uncertain significance not provided 2021-08-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002488818 SCV002776684 uncertain significance Medulloblastoma; Familial dysautonomia 2022-01-25 criteria provided, single submitter clinical testing
Natera, Inc. RCV000290763 SCV001458951 uncertain significance Familial dysautonomia 2020-09-16 no assertion criteria provided clinical testing

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