Variants
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rs115239774

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

19


Location

7639112


Variant Type

SNP

Genes

ClinVar

Name

NM_006949.4(STXBP2):c.169+12C>T


Allele

T


Clinical Significance

Benign

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