Variants
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rs8135665

  • not provided

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

38080269


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_013356.3(SLC16A8):c.1198+571G>A


Allele

T


Clinical Significance

not provided

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