"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SOX18"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 754921	NM_018419.3(SOX18):c.1149C>T (p.Ser383=)	SOX18	Single nucleotide variant (synonymous variant)	Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome +2 more	GLikely benign
Select item 765354	NM_018419.3(SOX18):c.1014C>G (p.Pro338=)	SOX18	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 261029	NM_018419.3(SOX18):c.243C>T (p.Asp81=)	SOX18	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign

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