ClinVar Miner

Submissions for variant NM_024411.5(PDYN):c.121A>G (p.Asn41Asp)

gnomAD frequency: 0.00258  dbSNP: rs59191035
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000518822 SCV000614431 benign not specified 2017-01-24 criteria provided, single submitter clinical testing
Invitae RCV000904758 SCV001049298 likely benign not provided 2023-12-07 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003905304 SCV004724283 benign PDYN-related condition 2019-02-21 criteria provided, single submitter clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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