Variants
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rs148458820

  • Affects

Your Genotype

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Description

Reference Allele

C


Alternative Allele

T

Chromosome

2


Location

219216803


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.717G>A (p.Trp239Ter)


Allele

T


Clinical Significance

Affects

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