List of variants in gene CASQ2 reported as benign for catecholaminergic polymorphic ventricular tachycardia 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001232.4(CASQ2):c.420+6T>C	rs9428083	0.71176
NM_001232.4(CASQ2):c.320-77C>T	rs7538337	0.70440
NM_001232.4(CASQ2):c.784-89C>T	rs2997742	0.58397
NM_001232.4(CASQ2):c.738-109G>A	rs4475752	0.51757
NM_001232.4(CASQ2):c.939+23C>T	rs3811003	0.39341
NM_001232.4(CASQ2):c.196A>G (p.Thr66Ala)	rs4074536	0.34486
NM_001232.3(CASQ2):c.-218T>C	rs78585518	0.09790
NM_001232.4(CASQ2):c.-137T>C	rs12069574	0.05139
NM_001232.4(CASQ2):c.731A>G (p.His244Arg)	rs28730716	0.02511
NM_001232.4(CASQ2):c.-21G>A	rs12067472	0.01521
NM_001232.4(CASQ2):c.226G>A (p.Val76Met)	rs10801999	0.01289
NM_001232.4(CASQ2):c.421-14G>A	rs139281637	0.00159
NM_001232.4(CASQ2):c.320-18C>T	rs376871374	0.00032
NM_001232.4(CASQ2):c.421-18G>C	rs202228431	0.00011
NM_001232.4(CASQ2):c.421-20A>T	rs201559752	0.00011
NM_001232.4(CASQ2):c.421-7A>T	rs776008006	0.00003
NM_001232.4(CASQ2):c.1185_1187del (p.Asp398del)	rs397516641
NM_001232.4(CASQ2):c.421-15C>G	rs199939582
NM_001232.4(CASQ2):c.738-12_738-5del	rs56889721
NM_001232.4(CASQ2):c.738-27dup	rs56889721
NM_001232.4(CASQ2):c.738-5del	rs56889721
NM_001232.4(CASQ2):c.738-6_738-5del	rs56889721
NM_001232.4(CASQ2):c.738-7_738-5del	rs56889721
NM_001232.4(CASQ2):c.738-8_738-5del	rs56889721
NM_001232.4(CASQ2):c.784-17T>A	rs2997741
NM_001232.4(CASQ2):c.784-17T>G	rs2997741

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