Variants
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rs57521028

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7610597


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_020902.2(CAMSAP3):c.882C>T (p.Tyr294=)


Allele

T


Clinical Significance

Benign

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