Variants
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rs770105416

  • Likely benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

22


Location

37973815


Variant Type

SNP

Genes

ClinVar

Name

NM_006941.4(SOX10):c.1081G>A (p.Ala361Thr)


Allele

T


Clinical Significance

Likely benign

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