Variants
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rs372865933

  • Uncertain significance

Your Genotype

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Description

Reference Allele

T


Alternative Allele

A

Chromosome

1


Location

115701395


Variant Type

SNP

Genes

ClinVar

Name

NM_001232.4(CASQ2):c.1046A>T (p.Asp349Val)


Allele

A


Clinical Significance

Uncertain significance

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