"PreventionGenetics, part of Exact Sciences"[submitter] AND "CALR3"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1046730	NM_145046.5(CALR3):c.1147G>A (p.Glu383Lys)	CALR3 (E383K)	Single nucleotide variant (missense variant)	CALR3-related disorder +1 more	GUncertain significance
Select item 955827	NM_145046.5(CALR3):c.641C>G (p.Ser214Trp)	CALR3 (S214W)	Single nucleotide variant (missense variant)	CALR3-related disorder +1 more	GUncertain significance
Select item 701233	NM_145046.5(CALR3):c.639A>G (p.Glu213=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19 +1 more	GLikely benign
Select item 471789	NM_145046.5(CALR3):c.493-6A>G	CALR3	Single nucleotide variant (intron variant)	CALR3-related disorder +2 more	GBenign/Likely benign
Select item 241951	NM_145046.5(CALR3):c.483C>A (p.Ile161=)	CALR3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 241949	NM_145046.5(CALR3):c.125A>G (p.Asn42Ser)	CALR3 (N42S)	Single nucleotide variant (missense variant)	CALR3-related disorder +2 more	GBenign/Likely benign
Select item 471797	NM_145046.5(CALR3):c.96T>C (p.His32=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19 +1 more	GBenign/Likely benign

ClinVar