"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "SNAP29"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1162872	NM_004782.4(SNAP29):c.16A>G (p.Lys6Glu)	SNAP29 (K6E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1162873	NM_004782.4(SNAP29):c.22T>C (p.Tyr8His)	SNAP29 (Y8H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1162874	NM_004782.4(SNAP29):c.51C>G (p.Asp17Glu)	SNAP29 (D17E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1162875	NM_004782.4(SNAP29):c.58G>C (p.Ala20Pro)	SNAP29 (A20P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1162876	NM_004782.4(SNAP29):c.145G>A (p.Val49Ile)	SNAP29 (V49I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1693774	NM_004782.4(SNAP29):c.318G>C (p.Gln106His)	SNAP29 (Q106H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 436825	NM_004782.4(SNAP29):c.629C>T (p.Ser210Phe)	SNAP29 (S210F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar