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rs10151259(G;T)

From SNPedia
Unaffected carrier of *possible* cone-rod mutation
Is agenotype
ofrs10151259
GeneRPGRIP1
Chromosome14
Position21,321,881
mentionedby
Magnitude1
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 1 Unaffected carrier of *possible* cone-rod mutation
(T;T) 2 Recessive genotype uncertain pathogenicity

see discussion at rs10151259