ClinVar Miner

Submissions for variant NM_000484.4(APP):c.1458+18C>T

dbSNP: rs200083249
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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 RCV002135924 SCV002451811 benign Alzheimer disease 2022-01-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494451 SCV002799909 likely benign Cerebral amyloid angiopathy, APP-related; Alzheimer disease type 1 2021-09-14 criteria provided, single submitter clinical testing

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