Related gene-specific medical variations for Gene (Select 9143) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545379	NM_004209.6(SYNGR3):c.56G>A (p.Ser19Asn)	LOC130058204, SYNGR3 (S19N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377158	NM_004209.6(SYNGR3):c.64C>T (p.Arg22Trp)	LOC130058204, SYNGR3 (R22W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234392	NM_004209.6(SYNGR3):c.18C>A (p.Phe6Leu)	LOC130058204, SYNGR3 (F6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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