ClinVar Miner

Submissions for variant NM_025216.2(WNT10A):c.-341A>G

gnomAD frequency: 0.00028  dbSNP: rs762914440
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000367457 SCV000427493 uncertain significance Odonto-onycho-dermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000275208 SCV000427494 uncertain significance SchC6pf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000327931 SCV000427495 uncertain significance Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing

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