ClinVar Miner

List of variants in gene TRAPPC2 reported as likely benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_001011658.4(TRAPPC2):c.*1229C>T rs141809461 0.00973
NM_001011658.4(TRAPPC2):c.*849C>T rs112880750 0.00172
NM_001011658.4(TRAPPC2):c.*710T>C rs141763219 0.00033
NM_001011658.4(TRAPPC2):c.*1050C>T rs184686872 0.00029
NM_001011658.4(TRAPPC2):c.*333G>A rs747205131 0.00003
NM_001011658.4(TRAPPC2):c.*1848dup rs200158505

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