Variants in gene PSEN2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 11

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HGVS	dbSNP	gnomAD frequency
NM_000447.3(PSEN2):c.903G>T (p.Thr301=)	rs6426553	0.03334
NM_000447.3(PSEN2):c.441C>T (p.Ser147=)	rs114334281	0.01441
NM_000447.3(PSEN2):c.185G>A (p.Arg62His)	rs58973334	0.01433
NM_000447.3(PSEN2):c.756G>C (p.Ala252=)	rs147702142	0.00621
NM_000447.3(PSEN2):c.1176C>T (p.Phe392=)	rs115652716	0.00524
NM_000447.3(PSEN2):c.861C>T (p.Pro287=)	rs75733498	0.00436
NM_000447.3(PSEN2):c.389C>T (p.Ser130Leu)	rs63750197	0.00073
NM_000447.3(PSEN2):c.336C>T (p.Tyr112=)	rs200610057	0.00050
NM_000447.3(PSEN2):c.754G>A (p.Ala252Thr)	rs138836272	0.00041
NM_000447.3(PSEN2):c.100G>A (p.Gly34Ser)	rs200636353	0.00019
NM_000447.3(PSEN2):c.149A>G (p.Gln50Arg)	rs143501870	0.00018

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