ClinVar Miner

Submissions for variant NM_003052.5(SLC34A1):c.1209C>T (p.Tyr403=)

dbSNP: rs1581648732
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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 RCV002096637 SCV002400023 likely benign not provided 2022-10-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499975 SCV002811891 likely benign Hypophosphatemic nephrolithiasis/osteoporosis 1; Fanconi renotubular syndrome 2; Hypercalcemia, infantile, 2 2021-07-22 criteria provided, single submitter clinical testing

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