Variants
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rs200339260

  • Uncertain significance

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

2


Location

219235545


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_018089.3(ANKZF1):c.1763T>C (p.Met588Thr)


Allele

C


Clinical Significance

Uncertain significance

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