List of variants in gene combination MYH11, NDE1 reported as pathogenic by Invitae

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
NC_000016.9:g.(?_15802668)_(15932109_?)del
NM_002474.3(MYH11):c.4116+1del	rs2151219190
NM_002474.3(MYH11):c.4179dup (p.Lys1394fs)
NM_002474.3(MYH11):c.4315C>T (p.Gln1439Ter)
NM_002474.3(MYH11):c.4401C>G (p.Tyr1467Ter)	rs8046180
NM_002474.3(MYH11):c.4578+1G>A	rs397514037
NM_002474.3(MYH11):c.4578+1G>C	rs397514037
NM_002474.3(MYH11):c.4578+1G>T	rs397514037
NM_002474.3(MYH11):c.5027_5028del (p.Lys1676fs)	rs1567692384
NM_002474.3(MYH11):c.5101_5102del (p.Arg1701fs)
NM_002474.3(MYH11):c.5599C>T (p.Gln1867Ter)	rs2151192622

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