List of variants in gene CCN6 reported as benign for bone development disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_198239.2(CCN6):c.168G>T (p.Gln56His)	rs1230345	0.32081
NM_198239.2(CCN6):c.-254A>G	rs3806964	0.25539
NM_198239.2(CCN6):c.72T>C (p.Thr24=)	rs1230346	0.04506
NM_198239.2(CCN6):c.807A>G (p.Gln269=)	rs17219737	0.04415
NM_198239.2(CCN6):c.178C>T (p.Arg60Cys)	rs17073260	0.03059
NM_198239.2(CCN6):c.237C>T (p.Ala79=)	rs112665393	0.01588
NM_198239.2(CCN6):c.78A>T (p.Pro26=)	rs9487806	0.01017
NM_198239.2(CCN6):c.366C>T (p.Cys122=)	rs112686348	0.00843
NM_198239.2(CCN6):c.892A>C (p.Ile298Leu)	rs34686812	0.00417
NM_198239.2(CCN6):c.248G>A (p.Gly83Glu)	rs147337485	0.00039

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