Related gene-specific medical variations for Gene (Select 6224) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3240379	NM_001023.4(RPS20):c.110C>G (p.Ala37Gly)	RPS20 (A37G)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 3240378	NM_001023.4(RPS20):c.236G>A (p.Arg79His)	RPS20 (R79H)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 2678456	NM_001023.4(RPS20):c.29C>T (p.Pro10Leu)	RPS20 (P10L)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 2678455	NM_001023.4(RPS20):c.133G>A (p.Glu45Lys)	RPS20 (E45K)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 2678454	NM_001023.4(RPS20):c.163C>G (p.Arg55Gly)	RPS20 (R55G)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 2678453	NM_001023.4(RPS20):c.5C>G (p.Ala2Gly)	RPS20 (A2G)	Single nucleotide variant (missense variant)	Hereditary nonpolyposis colon cancer	GUncertain significance
Select item 1259849	NM_001023.4(RPS20):c.104-90T>C	RPS20, SNORD54	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

ClinVar