Variants
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rs141262841

  • Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

22


Location

37973903


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.993C>T (p.Ser331=)


Allele

A


Clinical Significance

Likely benign

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