Variants
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rs1574808120

  • Likely benign

Your Genotype

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Description

Reference Allele

C


Alternative Allele

G

T

Chromosome

2


Location

219210235


Variant Type

SNP

Genes

Phenotypes

ClinVar

Name

NM_005689.4(ABCB6):c.2415G>A (p.Arg805=)


Allele

T


Clinical Significance

Likely benign

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