ClinVar Miner

Submissions for variant NM_173651.4(FSIP2):c.4459A>G (p.Ile1487Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003885824 SCV004700525 uncertain significance not provided 2024-02-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003949091 SCV004764118 benign FSIP2-related disorder 2023-01-24 no assertion criteria provided 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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