VAMP7[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57692	GRCh38/hg38 Xq28(chrX:155828359-155979369)x0	VAMP7	Copy number loss	See cases	GUncertain significance
Select item 777848	NM_005638.6(VAMP7):c.327C>G (p.Val109=)	VAMP7	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 795813	NM_005638.6(VAMP7):c.364G>A (p.Gly122Ser)	VAMP7 (G122S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 721652	NM_005638.6(VAMP7):c.380T>C (p.Met127Thr)	VAMP7 (M127T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2571389	NM_005638.6(VAMP7):c.585C>T (p.Ile195=)	VAMP7 (R173C)	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3036638	NM_005638.6(VAMP7):c.595-10G>C	VAMP7	Single nucleotide variant (intron variant)	VAMP7-related disorder	GBenign
Select item 154473	GRCh38/hg38 Yq12(chrY:56992525-57166951)x0	VAMP7	Copy number loss	See cases	GBenign
Select item 708966	NM_005638.6(VAMP7):c.573T>C (p.Ile191=)	VAMP7 (Y169H)	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign

ClinVar