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

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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.17175C>T (p.Thr5725=)	rs200002217	0.00011
NM_182961.4(SYNE1):c.16896+12A>G	rs1057522443	0.00001
NM_182961.4(SYNE1):c.16896+11dup	rs545568394
NM_182961.4(SYNE1):c.16984C>A (p.Arg5662Ser)	rs145899734
NM_182961.4(SYNE1):c.17019+16T>G	rs1554410174

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