List of variants in gene combination LOC126859836, SYNE1 reported as likely benign for Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.21612C>T (p.Pro7204=)	rs141170182	0.00013
NM_182961.4(SYNE1):c.21523-18G>T	rs191367384	0.00012
NM_182961.4(SYNE1):c.21523-11T>C	rs1467455394	0.00001
NM_182961.4(SYNE1):c.21523-19G>A	rs1480392957	0.00001
NM_182961.4(SYNE1):c.21523-6G>C	rs774046000	0.00001
NM_182961.4(SYNE1):c.21594A>G (p.Leu7198=)	rs750292751

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