Related gene-specific medical variations for Gene (Select 55168) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3208816	NM_018135.4(MRPS18A):c.517C>G (p.Arg173Gly)	MRPS18A, RSPH9 (R173G)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3208808	NM_018135.4(MRPS18A):c.502C>G (p.Arg168Gly)	MRPS18A, RSPH9 (R168G)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3208802	NM_018135.4(MRPS18A):c.482C>T (p.Pro161Leu)	MRPS18A, RSPH9 (P161L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3208800	NM_018135.4(MRPS18A):c.475G>A (p.Val159Ile)	MRPS18A, RSPH9 (V159I)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2467641	NM_018135.4(MRPS18A):c.505T>C (p.Trp169Arg)	MRPS18A, RSPH9 (W169R)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2455815	NM_018135.4(MRPS18A):c.562T>C (p.Ser188Pro)	RSPH9, MRPS18A (S188P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2411260	NM_018135.4(MRPS18A):c.526G>A (p.Val176Met)	MRPS18A, RSPH9 (V176M)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2359481	NM_018135.4(MRPS18A):c.542T>C (p.Leu181Pro)	MRPS18A, RSPH9 (L181P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2325800	NM_018135.4(MRPS18A):c.466C>T (p.Pro156Ser)	MRPS18A, RSPH9 (P156S)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2208139	NM_018135.4(MRPS18A):c.520A>G (p.Met174Val)	MRPS18A, RSPH9 (M174V)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance