ClinVar Miner

Submissions for variant NM_001136472.2(LITAF):c.27G>A (p.Ala9=)

gnomAD frequency: 0.00008  dbSNP: rs149518815
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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 RCV001083039 SCV000761152 likely benign Charcot-Marie-Tooth disease type 1C 2024-10-24 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000711268 SCV000841603 benign not provided 2018-05-02 criteria provided, single submitter clinical testing
GeneDx RCV000711268 SCV000984208 likely benign not provided 2018-04-18 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Ambry Genetics RCV002440271 SCV002745764 likely benign Inborn genetic diseases 2019-07-11 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.

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