Variants
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rs587784354

  • Likely pathogenic

Your Genotype

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Description

Reference Allele

A


Alternative Allele

T

Chromosome

22


Location

38112186


Variant Type

SNP

Genes

ClinVar

Name

NM_003560.4(PLA2G6):c.2396T>A (p.Leu799His)


Allele

T


Clinical Significance

Likely pathogenic

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