Related gene-specific medical variations for Gene (Select 8724) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3167267	NM_003795.6(SNX3):c.80A>C (p.Asn27Thr)	LOC129996937, SNX3 (N27T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490347	NM_003795.6(SNX3):c.11C>G (p.Thr4Ser)	LOC129996937, SNX3 (T4S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303714	NM_003795.6(SNX3):c.23C>G (p.Thr8Ser)	LOC129996937, SNX3 (T8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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