Variants
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rs1236012815

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

19


Location

7557191


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3304G>A (p.Ala1102Thr)


Allele

A


Clinical Significance

Likely pathogenic

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