Related gene-specific medical variations for Gene (Select 8876) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332129	NM_004666.3(VNN1):c.1366A>G (p.Thr456Ala)	LOC126859793, VNN1 (T456A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332126	NM_004666.3(VNN1):c.1375C>T (p.Arg459Cys)	LOC126859793, VNN1 (R459C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188715	NM_004666.3(VNN1):c.1360G>A (p.Val454Met)	LOC126859793, VNN1 (V454M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188714	NM_004666.3(VNN1):c.1333A>C (p.Asn445His)	LOC126859793, VNN1 (N445H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351329	NM_004666.3(VNN1):c.1219A>G (p.Asn407Asp)	LOC126859793, VNN1 (N407D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2308778	NM_004666.3(VNN1):c.1294G>A (p.Gly432Arg)	LOC126859793, VNN1 (G432R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2300723	NM_004666.3(VNN1):c.1345C>T (p.Pro449Ser)	LOC126859793, VNN1 (P449S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 749805	NM_004666.3(VNN1):c.1335T>C (p.Asn445=)	LOC126859793, VNN1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar