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rs1799989(A;C)

From SNPedia

benign most likely
Is agenotype
ofrs1799989
GeneTYR
Chromosome11
Position89,177,755
mentionedby
Magnitude0.5
ReputeBad
Geno Mag Summary
(A;C) 0.5 benign most likely
(C;C) 0 common in clinvar

although reported as an albinism allele, the frequency of this variant seems far too high in most populations to give credence to this.