List of variants in gene PSEN1 reported as likely benign for PSEN1-related disorder

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: 14

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HGVS	dbSNP	gnomAD frequency
NC_000014.9:g.73136191C>G	rs34086577	0.00339
NM_000021.4(PSEN1):c.1002C>T (p.Gly334=)	rs116640707	0.00037
NM_000021.4(PSEN1):c.1377A>G (p.Gln459=)	rs201496204	0.00009
NM_000021.4(PSEN1):c.909G>A (p.Pro303=)	rs377053325	0.00006
NM_000021.4(PSEN1):c.798T>A (p.Gly266=)	rs752833058	0.00001
NM_000021.4(PSEN1):c.*10G>A
NM_000021.4(PSEN1):c.1071A>G (p.Ser357=)
NM_000021.4(PSEN1):c.1248+7A>G
NM_000021.4(PSEN1):c.1272C>G (p.Leu424=)
NM_000021.4(PSEN1):c.223T>C (p.Leu75=)
NM_000021.4(PSEN1):c.468C>T (p.Tyr156=)
NM_000021.4(PSEN1):c.774A>G (p.Leu258=)
NM_000021.4(PSEN1):c.792G>T (p.Pro264=)	rs150301281
NM_000021.4(PSEN1):c.956-10T>C

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