Variants
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rs757292336

  • Likely benign
  • Likely benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

16


Location

2088514


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5328C>T (p.Ala1776=)


Allele

T


Clinical Significance

Likely benign

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