ClinVar Miner

Submissions for variant NM_025216.2(WNT10A):c.-400T>G

gnomAD frequency: 0.00738  dbSNP: rs556182426
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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 RCV000342611 SCV000427484 likely benign Selective tooth agenesis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000396361 SCV000427485 likely benign Odonto-onycho-dermal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000302946 SCV000427486 likely benign SchC6pf-Schulz-Passarge syndrome 2016-06-14 criteria provided, single submitter clinical testing

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