ClinVar Miner

Submissions for variant NM_002249.6(KCNN3):c.200AGC[19] (p.Gln76_Gln80dup)

dbSNP: rs3831942
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715288 SCV001940404 benign not provided 2020-11-25 criteria provided, single submitter clinical testing
Mendelics RCV002246459 SCV002517479 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506742 SCV002805387 benign Zimmermann-laband syndrome 3 2021-10-11 criteria provided, single submitter clinical testing

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