ClinVar Miner

Submissions for variant NM_003126.4(SPTA1):c.3314A>C (p.Asn1105Thr)

gnomAD frequency: 0.00001  dbSNP: rs200193956
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 RCV001881533 SCV002151567 benign not provided 2022-12-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001881533 SCV003820092 uncertain significance not provided 2022-09-23 criteria provided, single submitter clinical testing

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