Variants
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rs45517413

  • not provided

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

16


Location

2088297


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5231T>C (p.Leu1744Pro)


Allele

C


Clinical Significance

not provided

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