List of variants in gene combination OFD1, TRAPPC2 reported as uncertain significance for bone disorder

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001011658.4(TRAPPC2):c.-19-3T>C	rs781420575	0.00003
NM_001011658.4(TRAPPC2):c.-19-2_-19delinsGGA
NM_001011658.4(TRAPPC2):c.-19G>T	rs2518644633
NM_001011658.4(TRAPPC2):c.176T>C (p.Met59Thr)	rs2046291142

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