ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.4011+15T>G

gnomAD frequency: 0.00031  dbSNP: rs139032600
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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 RCV002146192 SCV002466504 benign Colorectal cancer, hereditary nonpolyposis, type 7 2024-08-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500326 SCV002798758 likely benign Endometrial carcinoma; Colorectal cancer, hereditary nonpolyposis, type 7; Colorectal cancer 2022-05-24 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003321911 SCV004027516 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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