ClinVar Miner

Submissions for variant NM_001177316.2(SLC34A3):c.870C>A (p.Gly290=)

dbSNP: rs747540875
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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 RCV002082851 SCV002327719 likely benign not provided 2024-12-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494013 SCV002795046 likely benign Autosomal recessive hypophosphatemic bone disease 2021-10-06 criteria provided, single submitter clinical testing

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