List of variants in gene combination CHRM2, LOC349160 reported as benign for Dilated Cardiomyopathy, Dominant

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001006630.2(CHRM2):c.*295T>A	rs8191992	0.59512
NM_001006630.2(CHRM2):c.1197T>C (p.Thr399=)	rs34586275	0.00676
NM_001006630.2(CHRM2):c.691G>A (p.Val231Ile)	rs76394680	0.00359
NM_001006630.2(CHRM2):c.773A>G (p.Asn258Ser)	rs142006633	0.00128
NM_001006630.2(CHRM2):c.1050A>G (p.Ser350=)	rs60372903	0.00070
NM_001006630.2(CHRM2):c.991A>T (p.Thr331Ser)	rs146328962	0.00064
NM_001006630.2(CHRM2):c.456C>T (p.Phe152=)	rs148163637	0.00038
NM_001006630.2(CHRM2):c.549T>C (p.Asn183=)	rs141951417	0.00031
NM_001006630.2(CHRM2):c.186A>G (p.Leu62=)	rs760443842	0.00001
NM_001006630.2(CHRM2):c.1107T>G (p.Thr369=)
NM_001006630.2(CHRM2):c.594A>G (p.Pro198=)	rs558678081

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