Variants
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rs776341298

  • Likely benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

C

Chromosome

2


Location

219235592


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_018089.3(ANKZF1):c.1803+7T>C


Allele

C


Clinical Significance

Likely benign

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