Variants
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rs370528124

  • Conflicting interpretations of pathogenicity

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

38112311


Variant Type

SNP

Genes

ClinVar

Name

NM_003560.4(PLA2G6):c.2277-6G>A


Allele

T


Clinical Significance

Conflicting interpretations of pathogenicity

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