Variants
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rs1862514

  • Benign

Your Genotype

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Description

Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: MAF

Reference Allele

C


Alternative Allele

T

Chromosome

19


Location

7633434


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_174895.3(PCP2):c.24G>A (p.Thr8=)


Allele

T


Clinical Significance

Benign

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