ClinVar Miner

Submissions for variant NM_025216.2(WNT10A):c.-203dup

dbSNP: rs561005501
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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 RCV000393221 SCV000427508 likely benign Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000312263 SCV000427509 likely benign Odonto-onycho-dermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000364629 SCV000427510 likely benign SchC6pf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing

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