ClinVar Miner

Submissions for variant NM_005592.4(MUSK):c.*153G>A

gnomAD frequency: 0.04940  dbSNP: rs111837461
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
GeneDx RCV001721942 SCV001949179 benign not provided 2018-11-16 criteria provided, single submitter clinical testing

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