ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.3280+8C>T

gnomAD frequency: 0.00007  dbSNP: rs544870680
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000655408 SCV000777338 likely benign Colorectal cancer, hereditary nonpolyposis, type 7 2023-12-04 criteria provided, single submitter clinical testing

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