List of variants in gene combination MYH11, NDE1 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.4861A>C (p.Lys1621Gln)	rs34321232	0.00011
NM_002474.3(MYH11):c.5406C>G (p.His1802Gln)	rs746211825	0.00010
NM_002474.3(MYH11):c.4200G>T (p.Glu1400Asp)	rs754997732	0.00001
NM_002474.3(MYH11):c.4543G>A (p.Asp1515Asn)	rs200909802	0.00001
NM_002474.3(MYH11):c.5089G>A (p.Ala1697Thr)	rs538145374	0.00001
NM_002474.3(MYH11):c.5095G>A (p.Ala1699Thr)	rs200410021	0.00001
NM_002474.3(MYH11):c.5299G>A (p.Glu1767Lys)	rs377663370	0.00001
NM_002474.3(MYH11):c.5302C>G (p.Gln1768Glu)	rs901502893	0.00001
NM_002474.3(MYH11):c.5485C>G (p.Gln1829Glu)	rs1005977032	0.00001
NM_017668.3(NDE1):c.948-3365C>T	rs374628714	0.00001
NM_002474.3(MYH11):c.4150G>A (p.Ala1384Thr)	rs775802674
NM_002474.3(MYH11):c.5222TGGAGGAGGAGC[3] (p.1741LEEE[3])	rs777249764
NM_002474.3(MYH11):c.5488G>A (p.Val1830Ile)	rs185904370
NM_002474.3(MYH11):c.5732C>G (p.Thr1911Arg)	rs748516947
NM_017668.3(NDE1):c.948-4460del	rs193922631
NM_017668.3(NDE1):c.948-5889A>G	rs193922632
NM_017668.3(NDE1):c.948-7057G>A	rs371348553

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