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Items: 3

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr12:111157990
GRCh38:
Chr12:110720185
PPP1CCnot providednot providedno assertion provided
2.
GRCh37:
Chr12:111169686
GRCh38:
Chr12:110731881
PPP1CCnot providednot providedno assertion provided
3.
GRCh37:
Chr12:111180507
GRCh38:
Chr12:110742702
PPP1CCnot providednot providedno assertion provided
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