List of variants in gene STARD7 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020151.4(STARD7):c.418C>T (p.Arg140Cys)	rs181733184	0.00006
NM_020151.4(STARD7):c.361C>T (p.Pro121Ser)	rs200880792	0.00005
NM_020151.4(STARD7):c.542A>G (p.Asn181Ser)

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