Variants
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rs73077102

  • Benign

Your Genotype

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Description

Reference Allele

T


Alternative Allele

A

C

Chromosome

2


Location

219237136


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_001286423.2(GLB1L):c.1901A>G (p.His634Arg)


Allele

C


Clinical Significance

Benign

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