Variants
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rs776008006

  • Benign/Likely benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

A

Chromosome

1


Location

115738342


Variant Type

SNP

Genes

ClinVar

Name

NM_001232.4(CASQ2):c.421-7A>T


Allele

A


Clinical Significance

Benign/Likely benign

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