Variants
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rs1483584740

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

A

G

Chromosome

22


Location

38112576


Variant Type

SNP

Genes

ClinVar

Name

NM_003560.4(PLA2G6):c.2204G>C (p.Cys735Ser)


Allele

G


Clinical Significance

Uncertain significance

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