ClinVar Miner

Submissions for variant NM_001177316.2(SLC34A3):c.1210+17G>A

dbSNP: rs202071967
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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 RCV001513349 SCV001720952 benign not provided 2025-01-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501778 SCV002803651 benign Autosomal recessive hypophosphatemic bone disease 2021-08-03 criteria provided, single submitter clinical testing

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