ClinVar Miner

Submissions for variant NC_012920.1(MT-CYB):m.15572T>C

dbSNP: rs207459996
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV002247304 SCV002516528 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
OMIM RCV000010315 SCV000030540 pathogenic Familial colorectal cancer 1998-11-01 no assertion criteria provided literature only

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