List of variants reported as uncertain significance for perceptual disorders by Reproductive Development, Murdoch Childrens Research Institute

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004837.4(GGPS1):c.782G>A (p.Arg261His)	rs1262402879	0.00008
NM_003201.3(TFAM):c.694C>T (p.Arg232Cys)	rs774009575	0.00001
NM_004837.4(GGPS1):c.269A>G (p.Asn90Ser)	rs1012843795
NM_052963.3(TOP1MT):c.1115G>C (p.Arg372Pro)	rs778858235

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