List of variants in gene combination LOC126859837, SYNE1 reported as likely benign by Athena Diagnostics

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.17052G>A (p.Pro5684=)	rs148994723	0.00010
NM_182961.4(SYNE1):c.17097C>T (p.Pro5699=)	rs769890058	0.00001
NM_182961.4(SYNE1):c.16770A>G (p.Leu5590=)
NM_182961.4(SYNE1):c.16984C>A (p.Arg5662Ser)	rs145899734
NM_182961.4(SYNE1):c.16984C>T (p.Arg5662Cys)	rs145899734

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