"PreventionGenetics, part of Exact Sciences"[submitter] AND "CLCC1"[ge - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 163641	NM_001377458.1(CLCC1):c.*2854T>C	CLCC1, GPSM2	Single nucleotide variant (3 prime UTR variant +2 more)	not specified +3 more	GBenign/Likely benign
Select item 3054619	NM_013296.5(GPSM2):c.1821C>T (p.Ser607=)	CLCC1, GPSM2	Single nucleotide variant (3 prime UTR variant +2 more)	GPSM2-related disorder	GLikely benign
Select item 211100	NM_013296.5(GPSM2):c.1909C>T (p.Arg637Trp)	CLCC1, GPSM2 (R637W)	Single nucleotide variant (3 prime UTR variant +2 more)	GPSM2-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 3029986	NM_013296.5(GPSM2):c.1983G>C (p.Gly661=)	CLCC1, GPSM2	Single nucleotide variant (3 prime UTR variant +2 more)	GPSM2-related disorder	GLikely benign
Select item 386577	NM_001377458.1(CLCC1):c.*2600A>G	GPSM2, CLCC1	Single nucleotide variant (3 prime UTR variant +1 more)	GPSM2-related disorder +2 more	GConflicting classifications of pathogenicity

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