Variants
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rs1394402504

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

A

Chromosome

22


Location

38112247


Variant Type

SNP

Genes

ClinVar

Name

NM_003560.4(PLA2G6):c.2335G>T (p.Val779Phe)


Allele

A


Clinical Significance

Uncertain significance

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