Related gene-specific medical variations for Gene (Select 6133) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046645	NM_000661.5(RPL9):c.-2+4A>G	LOC112939935, RPL9	Single nucleotide variant (intron variant)	RPL9-related disorder	GLikely benign
Select item 1300810	NM_000661.5(RPL9):c.-2+3A>G	LIAS, LOC112939935 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1294864	NM_000661.5(RPL9):c.-2+21G>C	LIAS, LOC112939935 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign

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