Related gene-specific medical variations for Gene (Select 10576) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2125542	NM_006431.3(CCT2):c.3+17T>G	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667083	NM_006431.3(CCT2):c.3+13C>A	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1655749	NM_006431.3(CCT2):c.3+16C>T	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1637984	NM_006431.3(CCT2):c.3+20C>T	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1579354	NM_006431.3(CCT2):c.3+7C>T	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1110698	NM_006431.3(CCT2):c.3+9G>A	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1015016	NM_006431.3(CCT2):c.3+6C>G	CCT2, LOC130008284	Single nucleotide variant (intron variant)	not provided	GUncertain significance

ClinVar