Variants
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rs187455529

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

38078399


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_013356.3(SLC16A8):c.1504G>A (p.Glu502Lys)


Allele

T


Clinical Significance

Benign

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