List of variants in gene combination CALM1, LOC126862021 reported as likely benign for catecholaminergic polymorphic ventricular tachycardia 4

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_006888.6(CALM1):c.402C>T (p.Asp134=)	rs193072150	0.00009
NM_006888.6(CALM1):c.417T>C (p.Tyr139=)	rs377521523	0.00001
NM_006888.6(CALM1):c.421+8_421+9del	rs767443947	0.00001
NM_006888.6(CALM1):c.422-16dup	rs776212211	0.00001
NM_006888.6(CALM1):c.422-20T>C	rs1232803707	0.00001
NM_006888.6(CALM1):c.426C>T (p.Phe142=)	rs199744595	0.00001
NM_006888.6(CALM1):c.390T>C (p.Asp130=)	rs2139771676
NM_006888.6(CALM1):c.405A>G (p.Gly135=)
NM_006888.6(CALM1):c.411C>A (p.Val137=)
NM_006888.6(CALM1):c.411C>G (p.Val137=)	rs749827346
NM_006888.6(CALM1):c.421+10A>G
NM_006888.6(CALM1):c.421+16C>G	rs267607279
NM_006888.6(CALM1):c.421+6dup	rs2139771726
NM_006888.6(CALM1):c.421+7_421+10del	rs771894805
NM_006888.6(CALM1):c.422-10G>A
NM_006888.6(CALM1):c.422-15T>C
NM_006888.6(CALM1):c.422-16_422-12del
NM_006888.6(CALM1):c.422-19A>G
NM_006888.6(CALM1):c.422-8C>T

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