Variants
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rs149202834

  • Benign/Likely benign

Your Genotype

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Description

Reference Allele

G


Alternative Allele

A

Chromosome

2


Location

219217783


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.574C>T (p.Arg192Trp)


Allele

A


Clinical Significance

Benign/Likely benign

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