Variants
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rs199579096

  • Benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

2


Location

219251616


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006000.3(TUBA4A):c.324T>C (p.Tyr108=)


Allele

G


Clinical Significance

Benign

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