List of variants in gene combination MYH11, NDE1 reported as uncertain significance by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.5470G>A (p.Ala1824Thr)	rs147710374	0.00036
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln)	rs34321232	0.00011
NM_017668.3(NDE1):c.948-3126G>A	rs377410503	0.00006
NM_002474.3(MYH11):c.4900G>A (p.Asp1634Asn)	rs549820613	0.00004
NM_002474.3(MYH11):c.4255G>C (p.Glu1419Gln)	rs567729923	0.00001
NM_002474.3(MYH11):c.5483A>T (p.Glu1828Val)	rs1365841164	0.00001
NM_002474.3(MYH11):c.5078A>G (p.Gln1693Arg)	rs1555551464
NM_002474.3(MYH11):c.5722G>A (p.Asp1908Asn)	rs1176411300

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