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rs80338869(A;C)

From SNPedia
Carrier of a spastic paraplegia 11 mutation
Is agenotype
ofrs80338869
GeneSPG11
Chromosome15
Position44,564,675
mentionedby
Magnitude3
ReputeBad
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