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rs63751243(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs63751243
GeneGRN
Chromosome17
Position44,349,190
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 3.8 Likely miscall in both 23andMe and Ancestry data; otherwise, possible frontotemporal dementia mutation
(C;C) 0 common in clinvar

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