ClinVar Miner

Submissions for variant NM_003052.5(SLC34A1):c.934C>T (p.Gln312Ter)

dbSNP: rs1554095568
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Shenzhen Institute of Pediatrics, Shenzhen Children's Hospital RCV000503372 SCV000590905 pathogenic Hypophosphatemic nephrolithiasis/osteoporosis 1 2017-08-11 criteria provided, single submitter clinical testing

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