ClinVar Miner

Submissions for variant NM_001110.4(ADAM10):c.510G>C (p.Gln170His)

gnomAD frequency: 0.00149  dbSNP: rs61751103
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002247474 SCV002516834 uncertain significance not specified 2022-05-04 criteria provided, single submitter clinical testing
OMIM RCV000077797 SCV000109631 risk factor Alzheimer disease 18 2013-10-16 no assertion criteria provided literature only

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