List of variants in gene combination MYH11, NDE1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.5439G>A (p.Lys1813=)	rs1050162	0.44262
NM_002474.3(MYH11):c.5478G>A (p.Leu1826=)	rs1050163	0.44235
NM_017668.3(NDE1):c.948-53G>A	rs7193920	0.07945
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=)	rs35295469	0.03116

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