Related gene-specific medical variations for Gene (Select 6173) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156079	NM_001199973.2(RPL36A-HNRNPH2):c.-16T>A	RPL36A, RPL36A-HNRNPH2	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3050211	NC_000023.11:g.101391265G>A	GLA, RPL36A +1 more	Single nucleotide variant (intron variant)	GLA-related disorder	GLikely benign
Select item 3048977	NC_000023.11:g.101391167A>G	GLA, RPL36A +1 more	Single nucleotide variant (intron variant)	GLA-related disorder	GLikely benign
Select item 3040732	NC_000023.11:g.101391195C>T	GLA, RPL36A +1 more	Single nucleotide variant (intron variant)	GLA-related disorder	GLikely benign
Select item 3031516	NC_000023.11:g.101391216G>A	GLA, RPL36A +1 more	Single nucleotide variant (intron variant)	GLA-related disorder	GLikely benign
Select item 708163	NM_021029.6(RPL36A):c.141C>T (p.Gly47=)	RPL36A, RPL36A-HNRNPH2	Single nucleotide variant (synonymous variant)	not provided	GBenign

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