Related gene-specific medical variations for Gene (Select 541578) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2661624	NM_001351114.2(HSFX4):c.939C>T (p.Tyr313=)	EOLA2, HSFX4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2661623	NM_001351114.2(HSFX4):c.306C>T (p.Asn102=)	EOLA2, HSFX4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 688189	GRCh37/hg19 Xq28(chrX:149028747-149519123)x2	EOLA2	Copy number gain	not provided	GUncertain significance

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