Related gene-specific medical variations for Gene (Select 51253) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296018	NM_016491.4(MRPL37):c.182C>T (p.Ala61Val)	LOC129930579, MRPL37 (A61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3207607	NM_016491.4(MRPL37):c.64G>A (p.Gly22Ser)	LOC129930579, MRPL37 (G22S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610860	NM_016491.4(MRPL37):c.133C>T (p.Pro45Ser)	LOC129930579, MRPL37 (P45S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331997	NM_016491.4(MRPL37):c.152A>T (p.Glu51Val)	LOC129930579, MRPL37 (E51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282178	NM_016491.4(MRPL37):c.184G>A (p.Gly62Arg)	LOC129930579, MRPL37 (G62R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279433	NM_016491.4(MRPL37):c.130C>T (p.Pro44Ser)	LOC129930579, MRPL37 (P44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar