ClinVar Miner

Submissions for variant NM_006361.6(HOXB13):c.602-4G>C

dbSNP: rs1214157618
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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 RCV001963628 SCV002254442 likely benign not provided 2022-08-09 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247316 SCV005895042 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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