List of variants in gene CCN6 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_198239.2(CCN6):c.589+27C>T	rs200472841	0.00047
NM_198239.2(CCN6):c.131G>A (p.Arg44His)	rs782703789	0.00011
NM_198239.2(CCN6):c.397C>G (p.Gln133Glu)
NM_198239.2(CCN6):c.6G>C (p.Gln2His)
NM_198239.2(CCN6):c.76C>G (p.Pro26Ala)	rs372990864

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