ClinVar Miner

Submissions for variant NM_002016.2(FLG):c.899_903del (p.Asp300fs)

dbSNP: rs1060499587
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
Division of Human Genetics, Children's Hospital of Philadelphia RCV000477947 SCV000536805 likely pathogenic Ichthyosis vulgaris 2015-12-04 no assertion criteria provided research

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