Variants
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rs1367848310

  • Likely benign

Your Genotype

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Description

Synonymous alterations with insufficient evidence to classify as benign

Reference Allele

C


Alternative Allele

G

T

Chromosome

16


Location

2088538


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5352C>T (p.Pro1784=)


Allele

T


Clinical Significance

Likely benign

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