Variants
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rs1377097612

  • Uncertain significance

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

Chromosome

2


Location

219211077


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.2000G>C (p.Gly667Ala)


Allele

G


Clinical Significance

Uncertain significance

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