"ADGRG2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3050062	NM_001079858.3(ADGRG2):c.2717-4G>T	ADGRG2	Single nucleotide variant (intron variant)	ADGRG2-related condition	GLikely benign
Select item 3042935	NM_001079858.3(ADGRG2):c.2028C>T (p.Asn676=)	ADGRG2	Single nucleotide variant (synonymous variant)	ADGRG2-related condition	GLikely benign
Select item 3035885	NM_001079858.3(ADGRG2):c.1653C>T (p.Asn551=)	ADGRG2	Single nucleotide variant (synonymous variant)	ADGRG2-related condition	GBenign
Select item 733038	NM_001079858.3(ADGRG2):c.1265+10C>T	ADGRG2	Single nucleotide variant (intron variant)	ADGRG2-related condition +1 more	GBenign/Likely benign
Select item 2629876	NM_001079858.3(ADGRG2):c.958C>T (p.Pro320Ser)	ADGRG2 (P282S +7 more)	Single nucleotide variant (missense variant)	ADGRG2-related condition	GUncertain significance
Select item 777787	NM_001079858.3(ADGRG2):c.870C>A (p.His290Gln)	ADGRG2 (H260Q +7 more)	Single nucleotide variant (missense variant)	ADGRG2-related condition +1 more	GBenign
Select item 3034185	NM_001079858.3(ADGRG2):c.102G>A (p.Leu34=)	ADGRG2	Single nucleotide variant (synonymous variant)	ADGRG2-related condition	GLikely benign

ClinVar