ClinVar Miner

Submissions for variant NM_000669.5(ADH1C):c.429C>T (p.Gly143=)

gnomAD frequency: 0.00180  dbSNP: rs79372027
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000888791 SCV001032444 benign not provided 2017-12-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000888791 SCV004153002 likely benign not provided 2022-08-01 criteria provided, single submitter clinical testing ADH1C: BP4, BP7

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