List of variants in gene CALR3 reported as uncertain significance for Hypertrophic cardiomyopathy

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_145046.5(CALR3):c.848C>T (p.Thr283Ile)	rs75099211	0.00138
NM_145046.5(CALR3):c.217C>G (p.Arg73Gly)	rs199561391	0.00005
NM_145046.5(CALR3):c.961G>A (p.Asp321Asn)	rs143334090	0.00001
NM_145046.5(CALR3):c.697C>G (p.Leu233Val)	rs2093383229

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