ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3557-17A>T

gnomAD frequency: 0.00004  dbSNP: rs542542093
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582946 SCV000690371 likely benign Hereditary cancer-predisposing syndrome 2015-07-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002497228 SCV002804555 likely benign Endometrial carcinoma; Lynch syndrome 5; Mismatch repair cancer syndrome 3 2022-03-31 criteria provided, single submitter clinical testing

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