Related gene-specific medical variations for Gene (Select 30817) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3242692	NC_000019.9:g.(?_14883134)_(14885138_?)del	ADGRE2	Deletion	not provided	GUncertain significance
Select item 3242691	NC_000019.9:g.(?_14884730)_(14887568_?)del	ADGRE2	Deletion	not provided	GUncertain significance
Select item 3242689	NC_000019.9:g.(?_14847048)_(14854616_?)del	ADGRE2	Deletion	not provided	GUncertain significance
Select item 156715	NM_013447.4(ADGRE2):c.478C>G (p.Leu160Val)	ADGRE2 (L160V)	Single nucleotide variant (missense variant)	not provided	Gnot provided

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