ClinVar Miner

List of variants in gene CCDC78 reported by GenomeConnect - Invitae Patient Insights Network

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001378030.1(CCDC78):c.436G>T (p.Val146Leu)	rs148705181	0.00014
NM_001378030.1(CCDC78):c.50G>A (p.Arg17Gln)	rs1046402338

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