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rs121907994(C;T)

From SNPedia
Carrier of a Wilson disease mutation
Is agenotype
ofrs121907994
GeneATP7B
Chromosome13
Position51,950,116
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a Wilson disease mutation

Unaffected in absence of a second ATP7B gene mutation; see links via main rs-page