ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.600C>T (p.Gly200=)

dbSNP: rs397517225
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000038762 SCV000062440 likely benign not specified 2011-12-27 criteria provided, single submitter clinical testing Gly200Gly in exon 4 of LDB3: This variant is not expected to have clinical signi ficance because it does not alter an amino acid residue and is not located withi n the splice consensus sequence. Gly200Gly in exon 4 of LDB3 (allele frequency = N/A)

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