"ADRA2B-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053525	NM_000682.7(ADRA2B):c.*2C>A	ADRA2B	Single nucleotide variant (3 prime UTR variant)	ADRA2B-related disorder	GLikely benign
Select item 3054220	NM_000682.7(ADRA2B):c.1233C>T (p.Phe411=)	ADRA2B	Single nucleotide variant (synonymous variant)	ADRA2B-related disorder	GLikely benign
Select item 3046238	NM_000682.7(ADRA2B):c.1126G>A (p.Val376Ile)	ADRA2B (V376I)	Single nucleotide variant (missense variant)	ADRA2B-related disorder	GLikely benign
Select item 3035246	NM_000682.7(ADRA2B):c.894AGAGGAGGA[3] (p.Glu309_Cys310insGluGluGlu)	ADRA2B	Microsatellite (inframe insertion)	ADRA2B-related disorder	GBenign
Select item 3029464	NM_000682.7(ADRA2B):c.783C>T (p.Thr261=)	ADRA2B	Single nucleotide variant (synonymous variant)	ADRA2B-related disorder	GLikely benign
Select item 3031914	NM_000682.7(ADRA2B):c.483C>T (p.Arg161=)	ADRA2B	Single nucleotide variant (synonymous variant)	ADRA2B-related disorder	GLikely benign
Select item 3035382	NM_000682.7(ADRA2B):c.36A>G (p.Thr12=)	ADRA2B	Single nucleotide variant (synonymous variant)	ADRA2B-related disorder	GBenign
Select item 3036697	NM_000682.7(ADRA2B):c.21C>T (p.Tyr7=)	ADRA2B	Single nucleotide variant (synonymous variant)	ADRA2B-related disorder	GLikely benign

ClinVar