Variants
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rs483352876

  • not provided

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

2


Location

219213280


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_005689.4(ABCB6):c.1766G>A (p.Arg589His)


Allele

T


Clinical Significance

not provided

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