ClinVar Miner

Submissions for variant NM_000227.6(LAMA3):c.150T>C (p.Tyr50=)

gnomAD frequency: 0.00007  dbSNP: rs770960237
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
PreventionGenetics, part of Exact Sciences RCV000246970 SCV000303061 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000932749 SCV001078436 benign not provided 2024-02-19 criteria provided, single submitter clinical testing

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