List of variants in gene combination MYH11, NDE1 reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=)	rs2075511	0.45713
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_002474.3(MYH11):c.3866T>C (p.Val1289Ala)	rs16967510	0.03954
NM_017668.3(NDE1):c.948-5739G>A	rs34839877	0.03595
NM_002474.3(MYH11):c.5370C>T (p.Leu1790=)	rs35295469	0.03116
NM_002474.3(MYH11):c.4158C>T (p.Thr1386=)	rs112377790	0.00746
NM_002474.3(MYH11):c.4522A>G (p.Met1508Val)	rs35176378	0.00480
NM_002474.3(MYH11):c.4239C>T (p.Ala1413=)	rs138573101	0.00226
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met)	rs7196804	0.00216
NM_017668.3(NDE1):c.948-2788A>G	rs118072250	0.00034

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