Related gene-specific medical variations for Gene (Select 90203) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3167229	NM_033421.4(SNX21):c.29T>C (p.Met10Thr)	LOC130065970, SNX21 (M10T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167228	NM_033421.4(SNX21):c.174C>A (p.Ser58Arg)	LOC130065971, SNX21 (S58R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557977	NM_033421.4(SNX21):c.4C>G (p.His2Asp)	LOC130065969, SNX21 (H2D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535017	NM_033421.4(SNX21):c.70G>A (p.Gly24Ser)	LOC130065970, SNX21 (G24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473994	NM_033421.4(SNX21):c.111G>C (p.Glu37Asp)	LOC130065970, SNX21 (E37D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295705	NM_033421.4(SNX21):c.31G>T (p.Ala11Ser)	LOC130065970, SNX21 (A11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar