List of variants in gene SACS reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.12649A>G (p.Asn4217Asp)	rs35799469	0.00744
NM_014363.6(SACS):c.8344G>A (p.Ala2782Thr)	rs61742502	0.00719
NM_014363.6(SACS):c.4118C>T (p.Ala1373Val)	rs61548169	0.00649

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