ClinVar Miner

Submissions for variant NM_001193315.2(VIPAS39):c.504+116A>T

gnomAD frequency: 0.02959  dbSNP: rs76597851
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001615704 SCV001835853 benign not provided 2019-07-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615704 SCV005295144 benign not provided criteria provided, single submitter not provided

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