Variants
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rs139460525

  • Benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

37833744


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_138797.4(ANKRD54):c.487C>T (p.Leu163=)


Allele

A


Clinical Significance

Benign

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