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rs104893915(C;T)

From SNPedia
carrier of one allele associated with several bone disorders
Is agenotype
ofrs104893915
GeneSLC26A2
Chromosome5
Position149,980,428
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of one allele associated with several bone disorders
(T;T) 7 Several bone disorders associated with this genotype

see discussion at rs104893915