ClinVar Miner

Submissions for variant NM_000393.5(COL5A2):c.2499+10A>G

dbSNP: rs886055356
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000308186 SCV000425640 uncertain significance Ehlers-Danlos syndrome type 7A 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003758751 SCV004526767 likely benign Ehlers-Danlos syndrome, classic type, 1 2023-07-30 criteria provided, single submitter clinical testing

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