Related gene-specific medical variations for Gene (Select 84144) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3172622	NM_032184.2(SYDE2):c.53C>G (p.Ala18Gly)	LOC129930865, SYDE2 (A18G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552245	NM_032184.2(SYDE2):c.237G>C (p.Met79Ile)	LOC129930865, SYDE2 (M79I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534655	NM_032184.2(SYDE2):c.76G>A (p.Ala26Thr)	LOC129930865, SYDE2 (A26T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534654	NM_032184.2(SYDE2):c.26G>T (p.Gly9Val)	LOC129930865, SYDE2 (G9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359209	NM_032184.2(SYDE2):c.101C>T (p.Ser34Phe)	LOC129930865, SYDE2 (S34F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353158	NM_032184.2(SYDE2):c.140G>A (p.Gly47Glu)	LOC129930865, SYDE2 (G47E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar