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rs201908137(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs201908137
GeneUNC13D
Chromosome17
Position75,840,506
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;C) 3 Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation
(C;C) 0 common in clinvar

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