ClinVar Miner

Submissions for variant NM_018706.7(DHTKD1):c.684T>C (p.Asn228=)

dbSNP: rs1564391006
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002085533 SCV002375173 likely benign 2-aminoadipic 2-oxoadipic aciduria 2021-08-07 criteria provided, single submitter clinical testing

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