List of variants in gene ST3GAL3 reported as likely benign for electroclinical syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_006279.5(ST3GAL3):c.530G>A (p.Arg177Gln)	rs780826701	0.00001
NM_006279.5(ST3GAL3):c.401A>G (p.Asn134Ser)	rs745451424

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