Variants in gene SYNE1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.21148C>T (p.Arg7050Ter)	rs763325410	0.00001
NM_182961.4(SYNE1):c.4561C>T (p.Arg1521Ter)	rs771760718	0.00001
NM_182961.4(SYNE1):c.7161del (p.Lys2388fs)	rs1220584620	0.00001
NM_182961.4(SYNE1):c.11971_11974del (p.Ile3991fs)	rs1246610728
NM_182961.4(SYNE1):c.16155C>G (p.Tyr5385Ter)
NM_182961.4(SYNE1):c.16390-2A>C	rs759460806
NM_182961.4(SYNE1):c.22709_22763del (p.Glu7570fs)	rs1554558620
NM_182961.4(SYNE1):c.4372_4373del (p.Leu1458fs)	rs794727577
NM_182961.4(SYNE1):c.639del (p.His214fs)	rs1412791793

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