Variants
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rs387906911

  • Pathogenic

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

2


Location

219218505


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.169G>A (p.Ala57Thr)


Allele

T


Clinical Significance

Pathogenic

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