Variants
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rs74566954

  • Benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

T

Chromosome

2


Location

219239841


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001286423.2(GLB1L):c.722-8T>A


Allele

T


Clinical Significance

Benign

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