ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.2285+10_2285+12del

dbSNP: rs562443353
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897412 SCV001041555 likely benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276417 SCV001462683 likely benign Familial hypokalemia-hypomagnesemia 2020-05-08 no assertion criteria provided clinical testing

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