Variants
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rs200506719

  • Benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

T

Chromosome

2


Location

219232564


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_018089.3(ANKZF1):c.439G>A (p.Glu147Lys)


Allele

A


Clinical Significance

Benign

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