Variants
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rs149363094

  • Benign/Likely benign

Your Genotype

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Description

See Variant Classification Assertion Criteria.

Reference Allele

G


Alternative Allele

A

C

Chromosome

2


Location

219213842


Variant Type

SNP

Genes

ClinVar

Name

NM_005689.4(ABCB6):c.1562C>G (p.Thr521Ser)


Allele

C


Clinical Significance

Benign/Likely benign

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