ClinVar Miner

Submissions for variant NM_025216.2(WNT10A):c.649G>A (p.Asp217Asn) (rs146902156)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000385003 SCV000427559 likely benign Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000271824 SCV000427560 likely benign Schopf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000322248 SCV000427561 likely benign Odontoonychodermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000023530 SCV000044821 pathogenic Tooth agenesis, selective, 4 2011-05-01 no assertion criteria provided literature only
UniProtKB/Swiss-Prot RCV000059804 SCV000091374 not provided not provided no assertion provided not provided

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