ClinVar Miner

List of variants reported as likely pathogenic for FGFR3-related chondrodysplasia by Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery,Institute of Otolaryngology, Chinese PLA General Hospital

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_000142.4(FGFR3):c.2287C>T (p.Leu763=) rs774517056

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