ClinVar Miner

Submissions for variant NM_001099667.3(ARMS2):c.298-14_298-13insG

gnomAD frequency: 0.01269  dbSNP: rs529644268
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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 RCV000271292 SCV000361196 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000271292 SCV000483040 likely benign Macular degeneration 2016-06-14 criteria provided, single submitter clinical testing

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