ClinVar Miner

Submissions for variant NM_017662.5(TRPM6):c.1224G>A (p.Ala408=)

dbSNP: rs141597109
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000907552 SCV001052262 likely benign not provided 2024-12-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502711 SCV002805719 likely benign Intestinal hypomagnesemia 1 2021-11-09 criteria provided, single submitter clinical testing

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