Related gene-specific medical variations for Gene (Select 84659) - ClinVar - NCBI

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Links from Gene

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3154856	NM_032572.4(RNASE7):c.280G>A (p.Asp94Asn)	NDRG2, RNASE7 (D94N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592754	NM_032572.4(RNASE7):c.265G>T (p.Ala89Ser)	NDRG2, RNASE7 (A89S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409012	NM_032572.4(RNASE7):c.190C>T (p.Arg64Trp)	NDRG2, RNASE7 (R64W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393747	NM_032572.4(RNASE7):c.460A>G (p.Arg154Gly)	NDRG2, RNASE7 (R154G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391006	NM_032572.4(RNASE7):c.429G>C (p.Gln143His)	NDRG2, RNASE7 (Q143H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317285	NM_032572.4(RNASE7):c.467T>C (p.Leu156Pro)	NDRG2, RNASE7 (L156P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299067	NM_032572.4(RNASE7):c.76G>C (p.Val26Leu)	NDRG2, RNASE7 (V26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294045	NM_032572.4(RNASE7):c.265G>A (p.Ala89Thr)	NDRG2, RNASE7 (A89T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2233943	NM_032572.4(RNASE7):c.191G>A (p.Arg64Gln)	NDRG2, RNASE7 (R64Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance