ClinVar Miner

Submissions for variant NM_001386125.1(OBSCN):c.144G>A (p.Gln48=)

gnomAD frequency: 0.01168  dbSNP: rs114375717
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000961358 SCV001108401 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV004029896 SCV002701835 likely benign not specified 2022-02-11 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Breakthrough Genomics, Breakthrough Genomics RCV000961358 SCV005281847 benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003916046 SCV004733671 benign OBSCN-related disorder 2019-02-21 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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