ClinVar Miner

List of variants in gene PLOD2 reported as likely benign for Bruck syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_000935.2(PLOD2):c.-212C>T rs564744346
NM_000935.2(PLOD2):c.-412C>T rs79723478
NM_182943.3(PLOD2):c.*171T>G rs13079521
NM_182943.3(PLOD2):c.*847C>T rs3792347

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