ClinVar Miner

Submissions for variant NM_000054.6(AVPR2):c.740G>A (p.Arg247His) (rs149668713)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514380 SCV000610339 likely benign not provided 2017-04-19 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000517077 SCV000612480 benign not specified 2017-04-26 criteria provided, single submitter clinical testing
Invitae RCV000514380 SCV001031896 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV001168115 SCV001330685 benign Nephrogenic diabetes insipidus, X-linked 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

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