Variants
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rs1599386139

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7637154


Variant Type

SNP

Genes

ClinVar

Name

NM_006949.4(STXBP2):c.5C>T (p.Ala2Val)


Allele

T


Clinical Significance

Uncertain significance

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