ClinVar Miner

Submissions for variant NM_001399.5(EDA):c.956G>T (p.Ser319Ile)

dbSNP: rs483352804
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genetic Disorders, Banaras Hindu University RCV000128525 SCV000148371 not provided Tooth agenesis, selective, X-linked, 1 no assertion provided not provided

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