List of variants in gene SYNE1 reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.21706G>A (p.Ala7236Thr)	rs202121741	0.00006
NM_182961.4(SYNE1):c.12272A>G (p.Asp4091Gly)	rs767294741	0.00001
NM_182961.4(SYNE1):c.22615C>T (p.Leu7539Phe)	rs768346744	0.00001
NM_182961.4(SYNE1):c.8374C>T (p.Arg2792Cys)	rs1249221823	0.00001
NM_182961.4(SYNE1):c.11446C>T (p.His3816Tyr)	rs761960802
NM_182961.4(SYNE1):c.12585G>A (p.Lys4195=)	rs149536991
NM_182961.4(SYNE1):c.263C>T (p.Ala88Val)	rs2154348376
NM_182961.4(SYNE1):c.8003A>G (p.Gln2668Arg)	rs2154133685

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