"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 262913	NM_175875.5(SIX5):c.2077G>A (p.Val693Met)	SIX5 (V693M)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 708639	NM_175875.5(SIX5):c.1963C>T (p.Leu655=)	SIX5	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 262912	NM_175875.5(SIX5):c.1903C>T (p.Pro635Ser)	SIX5 (P635S)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1285149	NM_175875.5(SIX5):c.1773G>T (p.Thr591=)	SIX5	Single nucleotide variant (synonymous variant)	Branchiootorenal syndrome 2 +1 more	GBenign/Likely benign
Select item 1285093	NM_175875.5(SIX5):c.1498G>A (p.Gly500Arg)	SIX5 (G500R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 708640	NM_175875.5(SIX5):c.150CGGGGC[3] (p.51GA[4])	DM1-AS, LOC107075317 +2 more	Microsatellite (inframe_insertion)	not provided	GBenign/Likely benign

ClinVar