ClinVar Miner

List of variants reported as uncertain significance for LADD syndrome

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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NM_000141.5(FGFR2):c.*736dup rs886046762
NM_000141.5(FGFR2):c.989G>A (p.Arg330Gln) rs199757302
NM_000142.5(FGFR3):c.1993G>T (p.Ala665Ser) rs764892330
NM_000142.5(FGFR3):c.200G>A (p.Gly67Asp) rs369232922
NM_000142.5(FGFR3):c.2153A>G (p.Asn718Ser) rs139773438
NM_004465.2(FGF10):c.541A>C (p.Asn181His) rs1332768200
NM_004465.2(FGF10):c.624A>G (p.Ser208=) rs886060653
NM_022970.3(FGFR2):c.110-22TC[3] rs773932794

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