List of variants in gene combination MYH11, NDE1 reported as benign by Illumina Laboratory Services, Illumina

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_017668.3(NDE1):c.*202G>A	rs11130	0.47916
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_017668.3(NDE1):c.*899C>A	rs79015533	0.11286
NM_017668.3(NDE1):c.*947G>A	rs760023	0.09015
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=)	rs12907	0.08987
NM_017668.3(NDE1):c.*913A>C	rs760024	0.08447
NM_017668.3(NDE1):c.*1299A>G	rs16967500	0.08018
NM_017668.3(NDE1):c.*1220G>A	rs74009414	0.08006
NM_017668.3(NDE1):c.*1389G>A	rs11557090	0.07983
NM_002474.3(MYH11):c.5517G>A (p.Ala1839=)	rs28505375	0.07791
NM_017668.3(NDE1):c.*1723C>T	rs73519694	0.06691
NM_002474.3(MYH11):c.3866T>C (p.Val1289Ala)	rs16967510	0.03954
NM_017668.3(NDE1):c.947+6711G>C	rs12932063	0.03681
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_017668.3(NDE1):c.947+6587C>T	rs116721094	0.01717
NM_017668.3(NDE1):c.*1784A>G	rs113405225	0.01698
NM_017668.3(NDE1):c.*2090T>C	rs140519946	0.00926
NM_017668.3(NDE1):c.*384C>T	rs193005461	0.00847
NM_002474.3(MYH11):c.4158C>T (p.Thr1386=)	rs112377790	0.00746
NM_002474.3(MYH11):c.3949C>A (p.Leu1317Ile)	rs141159831	0.00600
NM_017668.3(NDE1):c.*863C>G	rs12927605	0.00231
NM_002474.3(MYH11):c.3928G>A (p.Val1310Met)	rs7196804	0.00216
NM_002474.3(MYH11):c.4673C>T (p.Thr1558Met)	rs111854563	0.00078
NM_017668.3(NDE1):c.948-3127C>T	rs181115969	0.00022
NM_017668.3(NDE1):c.948-9103C>T	rs202120792	0.00006

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