List of variants reported as likely benign for Catecholaminergic polymorphic ventricular tachycardia by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_138959.3(VANGL1):c.*4478C>T	rs17034226	0.41876
NM_138959.3(VANGL1):c.*5751A>G	rs10801933	0.41406
NM_138959.3(VANGL1):c.*5368G>A	rs10494179	0.39762
NM_138959.3(VANGL1):c.*5995A>T	rs4595366	0.39755
NM_138959.3(VANGL1):c.*5841A>T	rs4548441	0.39752
NM_001232.4(CASQ2):c.1185C>T (p.Asp395=)	rs7413162	0.39681
NM_138959.3(VANGL1):c.*6026G>A	rs6428677	0.24227
NM_001232.4(CASQ2):c.1123_1124del	rs56839330	0.23414
NM_138959.3(VANGL1):c.*6199A>T	rs3811007	0.22923
NM_138959.3(VANGL1):c.*6212C>T	rs3811006	0.16816
NM_138959.3(VANGL1):c.*4504C>T	rs17034228	0.16812
NM_138959.3(VANGL1):c.*5266C>T	rs17034230	0.16811
NM_001232.4(CASQ2):c.*138T>C	rs28730710	0.10658
NM_138959.3(VANGL1):c.*6721A>G	rs17034249	0.10611
NM_138959.3(VANGL1):c.*6321T>G	rs77318780	0.06169
NM_001232.4(CASQ2):c.1194T>C (p.Asp398=)	rs28730711	0.04871
NM_001035.3(RYR2):c.8437-7dup	rs148246251	0.02544
NM_006073.4(TRDN):c.1805-5dup	rs755375052	0.02440
NM_001232.4(CASQ2):c.1014+9C>T	rs77775029	0.02121
NM_001232.4(CASQ2):c.1005T>C (p.Asn335=)	rs28730712	0.02116
NM_001035.3(RYR2):c.11880+13_11880+16del	rs199562036	0.01032
NM_001035.3(RYR2):c.9867G>A (p.Gly3289=)	rs190537182	0.00281
NM_001035.3(RYR2):c.4989C>T (p.Ala1663=)	rs147060179	0.00220
NM_001035.3(RYR2):c.*646del	rs377407067
NM_001035.3(RYR2):c.890_893dup	rs10667874
NM_001035.3(RYR2):c.4597-11del	rs3841805
NM_001232.4(CASQ2):c.*1017del	rs11347859
NM_138959.3(VANGL1):c.*5633T>G	rs4348723
NM_138959.3(VANGL1):c.*6763dup	rs5777244

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