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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr21:27269917
GRCh38:
Chr21:25897605
APPnot providedLikely pathogenic
(Apr 20, 2017)
criteria provided, single submitter
2.
GRCh37:
Chr21:27269917
GRCh38:
Chr21:25897605
APPnot providednot providedno assertion provided
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