List of variants in gene combination CASQ2, VANGL1 reported as likely benign for heart conduction disease

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: 21

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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_001232.4(CASQ2):c.1014+9C>T	rs77775029	0.02121
NM_001232.4(CASQ2):c.1005T>C (p.Asn335=)	rs28730712	0.02116
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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