List of variants in gene PSEN1 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_000021.4(PSEN1):c.932A>G (p.Lys311Arg)	rs115865530	0.00004
NM_000021.4(PSEN1):c.1087G>A (p.Glu363Lys)
NM_000021.4(PSEN1):c.584A>G (p.Tyr195Cys)

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