ClinVar Miner

Submissions for variant NM_001163809.2(WDR81):c.2142T>C (p.Gly714=)

gnomAD frequency: 0.23864  dbSNP: rs59643265
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004709292 SCV005251991 benign not provided criteria provided, single submitter not provided
Genetic Services Laboratory, University of Chicago RCV000118851 SCV000153505 likely benign not specified no assertion criteria provided clinical testing Likely benign based on allele frequency in 1000 Genomes Project or ESP global frequency and its presence in a patient with a rare or unrelated disease phenotype. NOT Sanger confirmed.

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