List of variants in gene PSEN1 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000021.4(PSEN1):c.1270C>G (p.Leu424Val)	rs1555358260
NM_000021.4(PSEN1):c.1303C>G (p.Leu435Val)	rs63750001
NM_000021.4(PSEN1):c.475T>C (p.Tyr159His)	rs1897961716
NM_000021.4(PSEN1):c.494G>T (p.Trp165Leu)	rs1898534725

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