ClinVar Miner

Submissions for variant NM_170754.4(TNS2):c.141A>G (p.Ala47=)

gnomAD frequency: 0.00065  dbSNP: rs113829803
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 RCV000916637 SCV001061883 benign not provided 2023-09-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000916637 SCV004133392 uncertain significance not provided 2023-10-01 criteria provided, single submitter clinical testing TNS2: PP3

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