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rs190166486(A;G)

From SNPedia
Carrier for a recessive mutation for deafness
Is agenotype
ofrs190166486
GenePTPRQ
Chromosome12
Position80,539,915
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 common/normal
(A;G) 3 Carrier for a recessive mutation for deafness

see PTPRQ gene for details