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rs104893922(A;A)

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common in clinvar

Is a	genotype
of	rs104893922
Gene	SMN1
Chromosome	5
Position	70,946,157
mentioned	by

0

Good

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	3	carrier of a spinal muscular atrophy disease allele
(G;G)	6	Spinal muscular atrophy, type 1

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Is a genotype