Variants
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rs796065353

  • Pathogenic

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

T

Chromosome

2


Location

219213495


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.1663C>A (p.Gln555Lys)


Allele

T


Clinical Significance

Pathogenic

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