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rs121907990(A;G)

From SNPedia
Carrier of a Wilson disease mutation
Is agenotype
ofrs121907990
GeneATP7B
Chromosome13
Position51,937,570
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Carrier of a Wilson disease mutation

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