List of variants in gene MYH15 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_014981.3(MYH15):c.5005C>T (p.Arg1669Cys)	rs76478083	0.00635
NM_014981.3(MYH15):c.3531T>C (p.Phe1177=)	rs201473403	0.00177
NM_014981.3(MYH15):c.2740C>T (p.Leu914=)
NM_014981.3(MYH15):c.2853A>C (p.Thr951=)
NM_014981.3(MYH15):c.294C>T (p.Ser98=)
NM_014981.3(MYH15):c.363G>A (p.Val121=)

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