ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1426A>T (p.Met476Leu)

dbSNP: rs200265913
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001054235 SCV001218539 likely benign Wilms tumor 1 2024-04-16 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV001507547 SCV001713155 uncertain significance not provided 2019-07-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005042230 SCV005683285 uncertain significance Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 1 2024-02-12 criteria provided, single submitter clinical testing
ITMI RCV000121185 SCV000085353 not provided not specified 2013-09-19 no assertion provided reference population

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