Variants
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rs45517417

  • not provided

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

16


Location

2088404


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5260-42C>T


Allele

T


Clinical Significance

not provided

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