"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "MED27"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2659637	NM_004269.4(MED27):c.682-3859T>C	MED27	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2659638	NM_004269.4(MED27):c.270G>A (p.Gly90=)	MED27	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2659639	NM_004269.4(MED27):c.150G>A (p.Lys50=)	MED27	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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