Variants
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rs11538945

  • Benign/Likely benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7639096


Variant Type

SNP

Genes

ClinVar

Name

NM_006949.4(STXBP2):c.165C>T (p.Ile55=)


Allele

T


Clinical Significance

Benign/Likely benign

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