Variants
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rs2091217625

  • Uncertain significance

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

16


Location

2088585


Variant Type

SNP

Genes

ClinVar

Name

NM_000548.5(TSC2):c.5399T>C (p.Val1800Ala)


Allele

C


Clinical Significance

Uncertain significance

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