List of variants in gene combination MYO5B, SNHG22 reported as likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001080467.3(MYO5B):c.*2538G>A	rs183150275	0.00425
NM_001080467.3(MYO5B):c.5395-6C>T	rs140275825	0.00317
NM_001080467.3(MYO5B):c.4481C>T (p.Ser1494Leu)	rs139632666	0.00202
NM_001080467.3(MYO5B):c.4674C>G (p.His1558Gln)	rs186428920	0.00105
NM_001080467.3(MYO5B):c.*1728A>T	rs138593222	0.00051
NM_001080467.3(MYO5B):c.*2571A>G	rs190516330	0.00027

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