List of variants in gene combination LOC129997480, SYNE1 reported as uncertain significance by Revvity Omics, Revvity

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.17512A>C (p.Thr5838Pro)	rs752135269	0.00009
NM_182961.4(SYNE1):c.17531C>G (p.Ser5844Cys)	rs144244988	0.00009
NM_182961.4(SYNE1):c.17519C>T (p.Ser5840Leu)	rs375874029	0.00003
NM_182961.4(SYNE1):c.17389T>C (p.Ser5797Pro)	rs753335678	0.00002
NM_182961.4(SYNE1):c.17347-3C>T	rs1424271720	0.00001
NM_182961.4(SYNE1):c.17401A>C (p.Lys5801Gln)	rs372368464	0.00001
NM_182961.4(SYNE1):c.17386_17387delinsAA (p.Ala5796Asn)	rs886043200
NM_182961.4(SYNE1):c.17501A>T (p.Glu5834Val)	rs2153813002
NM_182961.4(SYNE1):c.17509C>A (p.Pro5837Thr)	rs762353997

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