ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.174G>A (p.Glu58=)

dbSNP: rs1597934910
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002064418 SCV002459347 likely benign not provided 2024-11-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249109 SCV005895325 benign Prostate cancer, hereditary, 9 2024-10-29 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.
Laboratory of Virology, Microbiology, Quality and Medical Biotechnologies, Faculty of Sciences and Techniques - Mohammedia, Hassan II University of Casablanca RCV000855897 SCV000993888 uncertain significance Prostate cancer, hereditary, 1 no assertion criteria provided clinical testing

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