ClinVar Miner

Submissions for variant NM_003667.4(LGR5):c.2341C>G (p.Pro781Ala)

gnomAD frequency: 0.00718  dbSNP: rs113809442
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000950220 SCV001096508 benign not provided 2018-03-29 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000950220 SCV004135484 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing LGR5: BS2

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