"YBX1-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040692	NM_004559.5(YBX1):c.147C>T (p.Gly49=)	LOC129930347, YBX1	Single nucleotide variant (synonymous variant)	YBX1-related condition	GLikely benign
Select item 3035634	NM_004559.5(YBX1):c.507A>G (p.Glu169=)	YBX1	Single nucleotide variant (synonymous variant +1 more)	YBX1-related condition	GLikely benign
Select item 3053036	NM_004559.5(YBX1):c.680G>T (p.Gly227Val)	YBX1 (G227V)	Single nucleotide variant (missense variant +1 more)	YBX1-related condition	GBenign

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