ClinVar Miner

Submissions for variant NM_005689.4(ABCB6):c.1864-4A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005018656 SCV005647785 uncertain significance Familial pseudohyperkalemia; Langereis blood group; Microphthalmia, isolated, with coloboma 7; Dyschromatosis universalis hereditaria 3 2024-06-18 criteria provided, single submitter clinical testing

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