List of variants in gene combination MYH11, NDE1 reported as uncertain significance by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017668.3(NDE1):c.948-2772T>C	rs143288748	0.00138
NM_002474.3(MYH11):c.5275G>A (p.Val1759Ile)	rs138059405	0.00033
NM_001040113.2(MYH11):c.5822A>G (p.Gln1941Arg)	rs761957202	0.00001
NM_002474.3(MYH11):c.5052C>G (p.Ser1684Arg)	rs760908992
NM_002474.3(MYH11):c.5435_5440dup (p.Phe1812_Lys1813dup)	rs864309564

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