rs66469337(G;T)
From SNPedia
Carrier of an ornithine carbamoyltransferase mutation |
Is a | genotype |
of | rs66469337 |
Gene | OTC |
Chromosome | X |
Position | 38,421,050 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(G;G) | 8.2 | Ornithine Transcarbamylase Deficiency |
(G;T) | 3 | Carrier of an ornithine carbamoyltransferase mutation |
(T;T) | 0 | common in clinvar |
Usually unaffected in absence of a second OTC gene mutation; X-linked so primary risk is to sons. Note though that ~15% of carrier females become symptomatic during their lifetime.