ClinVar Miner

Submissions for variant NM_025216.2(WNT10A):c.-149G>T

gnomAD frequency: 0.00022  dbSNP: rs886055641
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000282018 SCV000427520 uncertain significance Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000318400 SCV000427521 uncertain significance Odonto-onycho-dermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000386984 SCV000427522 uncertain significance SchC6pf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694530 SCV005188288 uncertain significance not provided criteria provided, single submitter not provided

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