ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.7-331G>A

gnomAD frequency: 0.16236  dbSNP: rs77344209
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 RCV001608205 SCV001834038 benign not provided 2018-11-27 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001608205 SCV005303301 benign not provided criteria provided, single submitter not provided

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