ClinVar Miner

Submissions for variant NM_000092.5(COL4A4):c.3705A>G (p.Pro1235=)

gnomAD frequency: 0.00010  dbSNP: rs752638078
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000910462 SCV001055329 benign not provided 2024-01-28 criteria provided, single submitter clinical testing
GeneDx RCV000910462 SCV001934724 benign not provided 2020-05-18 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271499 SCV001452705 likely benign Alport syndrome 2020-05-02 no assertion criteria provided clinical testing

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