V460V[VARNAME] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 93451	NM_000157.4(GBA1):c.1497G>C (p.Val499=)	GBA1, LOC106627981	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 4297	NM_001005741.2(GBA1):c.[1448T>C;1483G>C;1497G>C]	GBA1, LOC106627981 (L483P +5 more)	Single nucleotide variant (missense variant +1 more)	Parkinson disease, late-onset +1 more	GPathogenic