Variants
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rs752945858

  • Benign/Likely benign

Your Genotype

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Description

Synonymous alterations with insufficient evidence to classify as benign

Reference Allele

C


Alternative Allele

A

T

Chromosome

16


Location

2088460


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5274C>T (p.Ala1758=)


Allele

T


Clinical Significance

Benign/Likely benign

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