Related gene-specific medical variations for Gene (Select 7434) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3188594	NM_003382.5(VIPR2):c.448C>T (p.Leu150Phe)	LOC126860263, VIPR2 (L134F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2658286	NM_003382.5(VIPR2):c.357+6853C>T	LOC110121203, VIPR2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2330369	NM_003382.5(VIPR2):c.427A>G (p.Thr143Ala)	LOC126860263, VIPR2 (T127A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 688886	GRCh37/hg19 7q36.3(chr7:158901052-159019897)x3	VIPR2	Copy number gain	not provided	GUncertain significance
Select item 684995	GRCh37/hg19 7q36.3(chr7:158920184-159038489)x3	VIPR2	Copy number gain	not provided	GUncertain significance
Select item 442173	GRCh37/hg19 7q36.3(chr7:158793641-159119707)x3	VIPR2	Copy number gain	See cases	GUncertain significance
Select item 394503	GRCh37/hg19 7q36.3(chr7:158850355-158935236)x3	VIPR2	Copy number gain	See cases	GBenign
Select item 157083	Single allele	VIPR2	Duplication	Normal pregnancy	Gnot provided

ClinVar