Variants
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rs45477298

  • not provided
  • Conflicting interpretations of pathogenicity

Your Genotype

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Description

Reference Allele

C


Alternative Allele

A

T

Chromosome

16


Location

2088462


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5276C>A (p.Ala1759Asp)


Allele

A


Clinical Significance

not provided

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