ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.4693C>T (p.Pro1565Ser)

gnomAD frequency: 0.00001  dbSNP: rs770278589
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002233203 SCV000817812 benign Ehlers-Danlos syndrome, classic type, 1 2025-01-19 criteria provided, single submitter clinical testing

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