ClinVar Miner

List of variants in gene CHRND reported as likely benign for autosomal recessive multiple pterygium syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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NM_000751.3(CHRND):c.*1025A>G rs115132742
NM_000751.3(CHRND):c.*424C>T rs4973046
NM_000751.3(CHRND):c.1047+9T>C rs3762528
NM_000751.3(CHRND):c.120G>A (p.Lys40=) rs55921262

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