List of variants in gene SNAP25 reported as likely benign by Ambry Genetics

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_130811.4(SNAP25):c.75G>T (p.Ser25=)	rs147866099	0.00128
NM_130811.4(SNAP25):c.6C>T (p.Ala2=)	rs11547858	0.00040
NM_130811.4(SNAP25):c.534C>T (p.Ile178=)	rs200030321	0.00025
NM_130811.4(SNAP25):c.366C>T (p.Asp122=)	rs377498338	0.00008
NM_130811.4(SNAP25):c.513C>T (p.Ile171=)	rs372122045	0.00005
NM_130811.4(SNAP25):c.462C>T (p.Ser154=)	rs201639889	0.00004
NM_130811.4(SNAP25):c.164-263C>T
NM_130811.4(SNAP25):c.24C>A (p.Arg8=)

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