List of variants in gene PSEN2 reported as uncertain significance by AiLife Diagnostics, AiLife Diagnostics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000447.3(PSEN2):c.-349-115A>G	rs556146007	0.00016
NM_000447.3(PSEN2):c.1160C>T (p.Thr387Ile)	rs867544084	0.00002
NM_000447.3(PSEN2):c.902C>T (p.Thr301Met)	rs144277432	0.00002
NM_000447.3(PSEN2):c.1139C>T (p.Thr380Met)	rs143912759
NM_000447.3(PSEN2):c.307G>A (p.Val103Ile)	rs2102672806

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