ClinVar Miner

Submissions for variant NM_145868.2(ANXA11):c.858+42CG[2]

dbSNP: rs746498821
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001643965 SCV001857353 benign not provided 2021-05-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260243 SCV002539320 benign Inclusion body myopathy and brain white matter abnormalities 2021-12-05 criteria provided, single submitter clinical testing

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