ClinVar Miner

Submissions for variant NM_001044385.3(TMEM237):c.1160-170T>C

gnomAD frequency: 0.07439  dbSNP: rs73989519
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 RCV001594806 SCV001828393 benign not provided 2018-07-06 criteria provided, single submitter clinical testing

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