ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.561A>G (p.Glu187=)

dbSNP: rs1597933795
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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 RCV003701347 SCV004455811 likely benign not provided 2025-01-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249610 SCV005894932 benign Prostate cancer, hereditary, 9 2024-10-30 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.

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