rs80338869(A;C)
From SNPedia
Carrier of a spastic paraplegia 11 mutation |
Is a | genotype |
of | rs80338869 |
Gene | SPG11 |
Chromosome | 15 |
Position | 44,564,675 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;C) | 3 | Carrier of a spastic paraplegia 11 mutation |
(C;C) | 0 | common in clinvar |
(C;T) | 0 | Benign variant according to ClinVar |
Unaffected in absence of a second SPG11 gene mutation