ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.2838A>T (p.Pro946=)

dbSNP: rs1576470760
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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 RCV001499786 SCV001704561 likely benign Ehlers-Danlos syndrome, type 4 2018-09-10 criteria provided, single submitter clinical testing

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