SNX24[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2379408	NM_014035.4(SNX24):c.128A>T (p.His43Leu)	SNX24 (H43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3167238	NM_014035.4(SNX24):c.206A>G (p.Lys69Arg)	SNX24 (K69R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284319	NM_014035.4(SNX24):c.259T>G (p.Leu87Val)	SNX24 (L87V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507846	NM_014035.4(SNX24):c.294T>G (p.Asp98Glu)	SNX24 (D98E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235897	NM_014035.4(SNX24):c.307C>G (p.Arg103Gly)	SNX24 (R103G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534095	NM_014035.4(SNX24):c.393G>C (p.Gln131His)	SNX24 (Q131H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516262	NM_014035.4(SNX24):c.430C>T (p.Pro144Ser)	SNX24 (P144S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2567299	NM_014035.4(SNX24):c.487T>A (p.Tyr163Asn)	SNX24 (Y163N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar