List of variants in gene combination MYH11, NDE1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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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.3700G>A (p.Ala1234Thr)	rs16967494	0.21955
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=)	rs12907	0.08987
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=)	rs28505375	0.07791
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_017668.3(NDE1):c.947+7126G>C	rs1875184	0.02929
NM_002474.3(MYH11):c.4770G>A (p.Lys1590=)	rs11648119	0.01341
NM_002474.3(MYH11):c.5676G>C (p.Glu1892Asp)	rs113964173	0.00462
NM_017668.3(NDE1):c.948-3127C>T	rs181115969	0.00022
NM_017668.3(NDE1):c.948-5748G>A	rs574893374	0.00001

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