Variants
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rs376664522

  • Affects

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

2


Location

219212413


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.1942C>T (p.Arg648Ter)


Allele

A


Clinical Significance

Affects

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