Variants
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rs61733629

  • Benign

Your Genotype

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Description

Reference Allele

A


Alternative Allele

G

Chromosome

2


Location

219214414


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_005689.4(ABCB6):c.1361T>C (p.Val454Ala)


Allele

G


Clinical Significance

Benign

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