ClinVar Miner

Submissions for variant NM_000035.4(ALDOB):c.156T>G (p.Thr52=)

gnomAD frequency: 0.00302  dbSNP: rs149671008
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241597 SCV000301583 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001722283 SCV000533838 likely benign not provided 2018-05-10 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000241597 SCV000706108 benign not specified 2017-02-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000966364 SCV001113678 benign Hereditary fructosuria 2025-02-03 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000966364 SCV003800559 likely benign Hereditary fructosuria 2022-03-07 criteria provided, single submitter clinical testing
Natera, Inc. RCV000966364 SCV002078725 likely benign Hereditary fructosuria 2019-12-10 no assertion criteria provided clinical testing

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