ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.93+8T>G

dbSNP: rs1567878012
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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 RCV000697304 SCV000825904 likely benign Familial cancer of breast; Fanconi anemia complementation group J 2024-02-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV000697304 SCV002812155 uncertain significance Familial cancer of breast; Fanconi anemia complementation group J 2021-07-11 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004788134 SCV005405856 likely benign Familial cancer of breast 2024-08-09 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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