Variants
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rs768125081

  • Uncertain significance

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

19


Location

7560687


Variant Type

SNP

Genes

ClinVar

Name

NM_001166114.2(PNPLA6):c.3739T>C (p.Trp1247Arg)


Allele

C


Clinical Significance

Uncertain significance

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