List of variants in gene combination MYH11, NDE1 reported as likely benign for Lissencephaly, Recessive

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_017668.3(NDE1):c.*899C>A	rs79015533	0.11286
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala)	rs16967510	0.03954
NM_017668.3(NDE1):c.948-5739G>A	rs34839877	0.03595
NM_017668.3(NDE1):c.*1784A>G	rs113405225	0.01698
NM_002474.3(MYH11):c.4401C>T (p.Tyr1467=)	rs8046180	0.01019
NM_017668.3(NDE1):c.*2090T>C	rs140519946	0.00926
NM_017668.3(NDE1):c.*384C>T	rs193005461	0.00847
NM_017668.3(NDE1):c.948-6839G>A	rs183176702	0.00636
NM_017668.3(NDE1):c.*863C>G	rs12927605	0.00231
NM_017668.3(NDE1):c.948-3127C>T	rs181115969	0.00022
NM_017668.3(NDE1):c.947+7069_947+7073del	rs5815842

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