List of variants in gene combination MYH8, MYHAS reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.714T>C (p.Thr238=)	rs8068729	0.86861
NM_002472.3(MYH8):c.2171+45G>A	rs2024076	0.63077
NM_002472.3(MYH8):c.3736-158C>G	rs3815314	0.56311
NM_002472.3(MYH8):c.5074T>C (p.Trp1692Arg)	rs8069834	0.50046
NM_002472.3(MYH8):c.806-139T>C	rs4791408	0.43008
NM_002472.3(MYH8):c.806-30T>C	rs4791406	0.42084
NM_002472.3(MYH8):c.512-123T>C	rs7216301	0.41553
NM_002472.3(MYH8):c.806-41T>C	rs4791407	0.40579
NM_002472.3(MYH8):c.1147+94C>T	rs11078845	0.38523
NM_002472.3(MYH8):c.1417-131G>A	rs12601678	0.36299
NM_002472.3(MYH8):c.1417-111C>T	rs12601552	0.36294
NM_002472.3(MYH8):c.-31G>A	rs2277648	0.30852
NM_002472.3(MYH8):c.5208C>T (p.Asp1736=)	rs33969260	0.17467
NM_002472.3(MYH8):c.1907C>T (p.Ala636Val)	rs34693726	0.05120
NM_002472.3(MYH8):c.2016C>T (p.Phe672=)	rs12936716	0.05000
NM_002472.3(MYH8):c.1416+131C>T	rs72816707	0.04312
NM_002472.3(MYH8):c.3862+174C>T	rs71358300	0.04263
NM_002472.3(MYH8):c.1701G>A (p.Gln567=)	rs73275411	0.01912
NM_002472.3(MYH8):c.4379A>G (p.Lys1460Arg)	rs112910113	0.00616
NM_002472.3(MYH8):c.2652A>G (p.Leu884=)	rs80168976	0.00605

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