Variants
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rs1176067979

  • Uncertain significance

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

19


Location

7558913


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3461A>G (p.Glu1154Gly)


Allele

G


Clinical Significance

Uncertain significance

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