Variants
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rs191487005

  • Benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

2


Location

219225104


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001077198.3(ATG9A):c.483C>T (p.His161=)


Allele

A


Clinical Significance

Benign

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