ClinVar Miner

Submissions for variant NM_006922.4(SCN3A):c.3449G>A (p.Arg1150Gln)

gnomAD frequency: 0.00006  dbSNP: rs775381308
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 RCV000805658 SCV000945622 likely benign not provided 2024-11-07 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000805658 SCV005876703 uncertain significance not provided 2024-03-12 criteria provided, single submitter clinical testing

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