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rs121907992(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121907992
GeneATP7B
Chromosome13
Position51,937,583
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 3 Carrier of a Wilson disease mutation
(G;G) 0 common in clinvar