ClinVar Miner

Submissions for variant NM_018206.6(VPS35):c.915-3del

dbSNP: rs569369937
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515864 SCV001724031 benign Parkinson disease 17 2020-08-05 criteria provided, single submitter clinical testing
Molecular Genetics, Royal Melbourne Hospital RCV003994142 SCV004812629 benign Parkinson disease 2023-05-04 criteria provided, single submitter clinical testing Latino/Admixed population allele frequency is 39.24% (rs746705076, 5847/14956 alleles, 0 homozygotes in gnomAD v2.1). Based on the classification scheme RMH Modified ACMG/AMP Guidelines v1.0, this variant is classified as BENIGN. Following criteria are met: BA1

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