List of variants in gene combination MYH8, MYHAS reported as likely benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.*76G>C	rs3744551	0.02944
NM_002472.3(MYH8):c.4233C>T (p.Asn1411=)	rs138992963	0.01251
NM_002472.3(MYH8):c.3686T>C (p.Met1229Thr)	rs35962914	0.00663
NM_002472.3(MYH8):c.3757C>T (p.Arg1253Cys)	rs34953692	0.00448
NM_002472.3(MYH8):c.805+9C>T	rs75468422	0.00426
NM_002472.3(MYH8):c.1632T>C (p.Pro544=)	rs144596237	0.00409
NM_002472.3(MYH8):c.*72T>C	rs184845947	0.00388
NM_002472.3(MYH8):c.4499C>T (p.Thr1500Met)	rs73977155	0.00334
NM_002472.3(MYH8):c.2274A>G (p.Gln758=)	rs145901155	0.00080
NM_002472.3(MYH8):c.1731G>C (p.Glu577Asp)	rs75160168	0.00053
NM_002472.3(MYH8):c.2117G>A (p.Arg706His)	rs150351713	0.00020
NM_002472.3(MYH8):c.1815T>A (p.Asn605Lys)	rs151091483	0.00012
NM_002472.3(MYH8):c.675C>T (p.Ser225=)	rs146651214	0.00009

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