ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.602-11A>G

dbSNP: rs749553801
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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 RCV002606763 SCV003503993 likely benign not provided 2024-10-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005248956 SCV005898746 likely benign Prostate cancer, hereditary, 9 2024-10-30 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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