ClinVar Miner

Submissions for variant NM_003737.4(DCHS1):c.3481+9A>T

gnomAD frequency: 0.00057  dbSNP: rs141566818
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897058 SCV001041177 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495429 SCV002795479 likely benign Van Maldergem syndrome 1; Mitral valve prolapse, myxomatous 2 2021-09-17 criteria provided, single submitter clinical testing

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