List of variants in gene SYNJ1 reported as likely benign by Athena Diagnostics Inc

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_203446.3(SYNJ1):c.43C>T (p.Pro15Ser)	rs61755328	0.00441
NM_203446.3(SYNJ1):c.*728C>T	rs2230767	0.00284
NM_203446.3(SYNJ1):c.1030G>A (p.Ala344Thr)	rs114942253	0.00255
NM_203446.3(SYNJ1):c.3590C>T (p.Thr1197Met)	rs145937537	0.00200
NM_203446.3(SYNJ1):c.3324G>A (p.Pro1108=)	rs757804939	0.00001
NM_203446.3(SYNJ1):c.3300C>T (p.Ala1100=)	rs2040034208

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