List of variants reported as likely pathogenic for perceptual disorders by Sydney Genome Diagnostics, Children's Hospital Westmead

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004183.4(BEST1):c.400C>G (p.Leu134Val)	rs753614067	0.00001
NM_000330.4(RS1):c.578C>A (p.Pro193His)	rs281865352
NM_001029883.3(PCARE):c.1984dup (p.Thr662fs)	rs1667504255

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