Variants
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rs780878126

  • Uncertain significance

Your Genotype

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Description

Reference Allele

G


Alternative Allele

T

Chromosome

19


Location

7559132


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3680G>T (p.Gly1227Val)


Allele

T


Clinical Significance

Uncertain significance

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