ClinVar Miner

Submissions for variant NM_025257.3(SLC44A4):c.1189C>T (p.Pro397Ser)

gnomAD frequency: 0.00789  dbSNP: rs116706632
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
GeneDx RCV001597797 SCV001831313 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001597797 SCV002403697 benign not provided 2025-01-23 criteria provided, single submitter clinical testing

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