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rs587782069(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs587782069
GeneFLCN
Chromosome17
Position17,224,041
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 5 Birt-Hogg-Dube Syndrome

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