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rs768729972(-;A)

From SNPedia
Carrier of a Wilson disease mutation
Is agenotype
ofrs768729972
GeneATP7B
Chromosome13
Position51,958,500
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 3 Carrier of a Wilson disease mutation

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