Variants
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rs1397403248

  • Uncertain significance

Your Genotype

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Description

This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

37973731


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_006941.4(SOX10):c.1165G>A (p.Gly389Ser)


Allele

T


Clinical Significance

Uncertain significance

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