Variants
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rs1202026658

  • Uncertain significance

Your Genotype

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Description

In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7557201


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3314C>T (p.Thr1105Met)


Allele

T


Clinical Significance

Uncertain significance

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