ClinVar Miner

Submissions for variant NM_013447.4(ADGRE2):c.1693_1709del (p.Gln565fs)

dbSNP: rs375427337
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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 RCV000879917 SCV001022973 likely benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495337 SCV002798087 likely benign Vibratory urticaria 2022-02-10 criteria provided, single submitter clinical testing

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