ClinVar Miner

Submissions for variant NM_000021.3(PSEN1):c.-241G>T

dbSNP: rs886050661
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000333397 SCV000388084 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000381109 SCV000388085 uncertain significance Early-onset autosomal dominant Alzheimer disease 2016-06-14 criteria provided, single submitter clinical testing

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