List of variants in gene SIX1 reported as pathogenic for perceptual disorders

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005982.4(SIX1):c.328C>T (p.Arg110Trp)	rs80356459
NM_005982.4(SIX1):c.337C>T (p.Arg113Ter)
NM_005982.4(SIX1):c.340A>G (p.Lys114Glu)
NM_005982.4(SIX1):c.373G>A (p.Glu125Lys)	rs797044960
NM_005982.4(SIX1):c.386A>C (p.Tyr129Ser)	rs104894478
NM_005982.4(SIX1):c.386A>G (p.Tyr129Cys)	rs104894478
NM_005982.4(SIX1):c.396G>C (p.Lys132Asn)	rs1303947821
NM_005982.4(SIX1):c.397_399del (p.Glu133del)	rs80356460
NM_005982.4(SIX1):c.746C>T (p.Pro249Leu)	rs368974927

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