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rs80338869(C;C)

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common in clinvar

Is a	genotype
of	rs80338869
Gene	SPG11
Chromosome	15
Position	44,564,675
mentioned	by

0

Good

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

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Is a genotype