ClinVar Miner

Submissions for variant NM_001145809.2(MYH14):c.5384G>A (p.Arg1795His)

dbSNP: rs567922009
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV001129869 SCV001289422 uncertain significance Autosomal dominant nonsyndromic hearing loss 4A 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. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.
Fulgent Genetics, Fulgent Genetics RCV002505705 SCV002814101 uncertain significance Autosomal dominant nonsyndromic hearing loss 4A; Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome 2021-12-10 criteria provided, single submitter clinical testing

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