"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SIX1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 751952	NM_005982.4(SIX1):c.816C>T (p.Leu272=)	SIX1	Single nucleotide variant (synonymous variant)	Branchiootic syndrome 3 +2 more	GLikely benign
Select item 1331163	NM_005982.4(SIX1):c.615T>G (p.Pro205=)	SIX1	Single nucleotide variant (synonymous variant)	Branchiootic syndrome 3 +3 more	GBenign/Likely benign
Select item 466172	NM_005982.4(SIX1):c.474C>T (p.Ala158=)	SIX1	Single nucleotide variant (synonymous variant)	Branchiootic syndrome 3 +3 more	GLikely benign
Select item 703043	NM_005982.4(SIX1):c.465G>A (p.Arg155=)	SIX1	Single nucleotide variant (synonymous variant)	Branchiootic syndrome 3 +2 more	GLikely benign
Select item 8308	NM_005982.4(SIX1):c.386A>G (p.Tyr129Cys)	SIX1 (Y129C)	Single nucleotide variant (missense variant)	Branchiootic syndrome +4 more	GPathogenic
Select item 227075	NM_005982.4(SIX1):c.162G>A (p.Ala54=)	SIX1	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 23 +4 more	GBenign/Likely benign

ClinVar