Variants
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rs778705470

  • Uncertain significance
  • no interpretation for the single variant

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

22


Location

38112226


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_003560.4(PLA2G6):c.2356G>C (p.Glu786Gln)


Allele

G


Clinical Significance

Uncertain significance

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