List of variants in gene SIX1 reported as likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005982.4(SIX1):c.316G>T (p.Val106Leu)	rs2140241235
NM_005982.4(SIX1):c.329G>T (p.Arg110Leu)	rs1064794308
NM_005982.4(SIX1):c.353C>T (p.Pro118Leu)
NM_005982.4(SIX1):c.373G>A (p.Glu125Lys)	rs797044960
NM_005982.4(SIX1):c.385T>C (p.Tyr129His)
NM_005982.4(SIX1):c.397_399del (p.Glu133del)	rs80356460
NM_005982.4(SIX1):c.460A>T (p.Lys154Ter)	rs1060499595

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