Variants
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rs189368660

  • Benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

A

Chromosome

19


Location

7632826


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_174895.3(PCP2):c.56G>T (p.Gly19Val)


Allele

A


Clinical Significance

Benign

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