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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000447.3(PSEN2):c.336C>T (p.Tyr112=)	rs200610057	0.00050
NM_000447.3(PSEN2):c.690C>G (p.Ala230=)	rs145010538	0.00033
NM_000447.3(PSEN2):c.166G>A (p.Gly56Ser)	rs188598190	0.00018
NM_000447.3(PSEN2):c.300C>T (p.Ile100=)	rs200801915	0.00010
NM_000447.3(PSEN2):c.208G>A (p.Gly70Arg)	rs139972151	0.00005
NM_000447.3(PSEN2):c.415G>A (p.Val139Met)	rs202178897	0.00003

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