List of variants in gene ADRA2B 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000682.7(ADRA2B):c.274G>A (p.Asp92Asn)	rs1397681630
NM_000682.7(ADRA2B):c.649G>A (p.Glu217Lys)	rs371934652
NM_000682.7(ADRA2B):c.664C>T (p.Arg222Ter)	rs786205528
NM_000682.7(ADRA2B):c.675_686delinsGTTTGGCAG (p.His225_Leu229delinsGlnPheGlyArg)	rs879255577

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