ClinVar Miner

List of variants in gene CDH1 reported as uncertain significance for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.1926C>A (p.Tyr642Ter) rs1961172043
NM_004360.5(CDH1):c.895G>A (p.Ala299Thr) rs1960837744

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