List of variants in gene MYH7 reported as benign for congenital anomaly of cardiovascular system

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.-9+23T>C	rs2239578	0.51695
NM_000257.4(MYH7):c.189C>T (p.Thr63=)	rs2069540	0.51584
NM_000257.4(MYH7):c.2967T>C (p.Ile989=)	rs7157716	0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542	0.27385
NM_000257.4(MYH7):c.1128C>T (p.Asp376=)	rs2231126	0.15761
NM_000257.4(MYH7):c.1095G>A (p.Lys365=)	rs735711	0.13859
NM_000257.4(MYH7):c.1767C>T (p.Asn589=)	rs3729816	0.01311
NM_000257.4(MYH7):c.3972+16G>A	rs114978322	0.00424
NM_000257.4(MYH7):c.2162+4G>A	rs145738465	0.00276
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr)	rs145532615	0.00095
NM_000257.4(MYH7):c.4005G>A (p.Ser1335=)	rs144465613	0.00064
NM_000257.4(MYH7):c.3036C>T (p.Ala1012=)	rs145379951	0.00050
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr)	rs45478699	0.00013
NM_000257.4(MYH7):c.3337-4dup	rs45504498

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