Variants
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rs387906910

  • Pathogenic

Your Genotype

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Description

Reference Allele

G


Alternative Allele

C

Chromosome

2


Location

219210036


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.2431C>G (p.Leu811Val)


Allele

C


Clinical Significance

Pathogenic

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