List of variants in gene MYH14 reported as uncertain significance by Kariminejad - Najmabadi Pathology & Genetics Center

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.5504G>A (p.Arg1835His)	rs754861302	0.00005
NM_001145809.2(MYH14):c.4310G>A (p.Arg1437His)	rs766518836	0.00001
NM_001145809.2(MYH14):c.3514C>T (p.Arg1172Trp)	rs373919106

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