List of variants in gene CALR3 reported as benign for cardiovascular disorder

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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: 23

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HGVS	dbSNP	gnomAD frequency
NM_145046.5(CALR3):c.381G>A (p.Gln127=)	rs3810198	0.66498
NM_145046.5(CALR3):c.972C>T (p.Tyr324=)	rs9305079	0.65389
NM_145046.5(CALR3):c.702C>T (p.Asp234=)	rs10403020	0.16282
NM_145046.5(CALR3):c.397+10C>T	rs3810197	0.12582
NM_145046.5(CALR3):c.820G>A (p.Val274Ile)	rs12459238	0.02726
NM_145046.5(CALR3):c.861G>A (p.Thr287=)	rs118131979	0.01186
NM_145046.5(CALR3):c.850G>A (p.Asp284Asn)	rs10404156	0.00473
NM_145046.5(CALR3):c.1012-9T>C	rs144370982	0.00268
NM_145046.5(CALR3):c.483C>A (p.Ile161=)	rs143158265	0.00190
NM_145046.5(CALR3):c.848C>T (p.Thr283Ile)	rs75099211	0.00138
NM_145046.5(CALR3):c.125A>G (p.Asn42Ser)	rs149634686	0.00123
NM_145046.5(CALR3):c.398-6T>C	rs376479901	0.00118
NM_145046.5(CALR3):c.398-4G>A	rs374008030	0.00040
NM_145046.5(CALR3):c.60C>G (p.Thr20=)	rs370721650	0.00029
NM_145046.5(CALR3):c.243C>T (p.Phe81=)	rs201321577	0.00014
NM_145046.5(CALR3):c.594C>T (p.Tyr198=)	rs145046810	0.00004
NM_145046.5(CALR3):c.1087C>T (p.Leu363=)	rs199900092	0.00003
NM_145046.5(CALR3):c.96T>C (p.His32=)	rs144355944	0.00001
NM_145046.5(CALR3):c.1067G>T (p.Arg356Leu)	rs140290452
NM_145046.5(CALR3):c.194-13A>G
NM_145046.5(CALR3):c.493-6A>G	rs566199743
NM_145046.5(CALR3):c.787-14dup	rs1267486642
NM_145046.5(CALR3):c.813T>C (p.His271=)

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