ClinVar Miner

Submissions for variant NM_004252.5(NHERF1):c.107G>A (p.Gly36Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, Biobizkaia Health Research Institute RCV003984464 SCV004708204 uncertain significance Hypophosphatemic nephrolithiasis/osteoporosis 2 2024-03-08 no assertion criteria provided clinical testing

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