Variants
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rs1569239288

  • Uncertain significance

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

22


Location

38112532


Variant Type

SNP

Genes

ClinVar

Name

NM_003560.4(PLA2G6):c.2248T>C (p.Cys750Arg)


Allele

G


Clinical Significance

Uncertain significance

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