List of variants in gene CCNQ studied for bone disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NC_000023.11:g.153585471_153589719del
NM_152274.5(CCNQ):c.303dup (p.Asn102Ter)	rs1569536891
NM_152274.5(CCNQ):c.651G>A (p.Trp217Ter)	rs2148299424
NM_152274.5(CCNQ):c.657+1G>A	rs1569536789
NM_152274.5(CCNQ):c.658-1G>A	rs63749972

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