Variants
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rs1000008449

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

19


Location

7560692


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3744C>G (p.Ser1248Arg)


Allele

G


Clinical Significance

Uncertain significance

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