ClinVar Miner

Submissions for variant NM_024915.4(GRHL2):c.1806G>A (p.Ser602=)

dbSNP: rs61732855
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
Athena Diagnostics RCV000711853 SCV000842259 benign not provided 2018-05-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000711853 SCV005744988 likely benign not provided 2024-03-14 criteria provided, single submitter clinical testing

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