ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.18G>A (p.Thr6=)

dbSNP: rs576539291
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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 RCV002110632 SCV002431797 likely benign Alagille syndrome due to a JAG1 point mutation 2021-10-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV002409561 SCV002723628 likely benign Cardiovascular phenotype 2022-09-02 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.

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