ClinVar Miner

Submissions for variant NM_004963.4(GUCY2C):c.1283-16G>T

dbSNP: rs112926992
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514618 SCV000610022 likely benign not provided 2017-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514618 SCV002414940 benign not provided 2023-12-12 criteria provided, single submitter clinical testing

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